Gloves are designed to safeguard hands from various hazards in industrial environments. They are commonly used to protect against chemicals, abrasions, cuts, and extreme temperatures. Key industries that rely on gloves include manufacturing, construction, healthcare, and food processing. These gloves come in various materials such as latex, nitrile, and leather, each offering specific benefits like chemical resistance, durability, and dexterity. By selecting the appropriate type of glove, businesses can enhance worker safety and maintain compliance with industry standards.

Packaging Supplies, also known as packing materials or shipping supplies, encompass a wide range of products designed to protect, contain, and transport goods efficiently. These supplies include items such as boxes, bubble wrap, packing peanuts, tape, and pallets. Key industries that rely heavily on packaging supplies include manufacturing, logistics, e-commerce, food and beverage, pharmaceuticals, and retail. These materials are essential for ensuring product safety, reducing damage during transit, and optimizing storage and handling processes.

Safety Equipment, also known as Personal Protective Equipment (PPE), encompasses a range of products designed to protect workers from hazards in the workplace. This category includes items such as helmets, gloves, goggles, hearing protection, and respiratory masks. Key industries that rely heavily on safety equipment include construction, manufacturing, oil and gas, mining, and chemical processing. These products are essential for ensuring worker safety and compliance with industry regulations.

Workwear, also known as industrial clothing or protective apparel, encompasses a range of garments designed to ensure safety, durability, and comfort for workers in demanding environments. Commonly used in industries such as construction, manufacturing, oil and gas, and utilities, workwear includes items like coveralls, high-visibility vests, flame-resistant clothing, and safety footwear. These products are essential for protecting workers from hazards, enhancing visibility, and maintaining compliance with safety regulations.

Food Service & Restaurant Supplies encompass a wide range of products essential for the efficient operation of food establishments. This category, also known as commercial kitchen supplies or foodservice equipment, includes items such as cookware, utensils, and storage solutions. Key industries that rely on these supplies include restaurants, catering services, hotels, and institutional food service providers such as schools and hospitals. These products are crucial for maintaining high standards of food safety, hygiene, and operational efficiency.

Cleaning & Hygiene Supplies, also known as janitorial supplies or sanitation products, encompass a wide range of items designed to maintain cleanliness and promote health in various environments. This category includes cleaning chemicals, disinfectants, paper products, hand sanitizers, and cleaning equipment such as mops and vacuum cleaners. Key industries that rely on these supplies include healthcare, manufacturing, food processing, hospitality industry, and education. These products are essential for ensuring a safe and sanitary environment, helping to prevent the spread of contaminants and maintain operational efficiency.

Tools, Tapes & Bolts encompass a wide range of essential items used for construction, maintenance, and repair tasks across various industries. This category includes hand tools, power tools, adhesive tapes, and fasteners such as bolts, screws, and nuts. Commonly referred to as hardware supplies or fastening solutions, these products are indispensable in sectors like manufacturing, construction, automotive, and aerospace. They ensure the structural integrity and functionality of machinery, buildings, and vehicles, making them critical for procurement buyers focused on quality and reliability.

Kolmi Mass Balance Oxygen Mask FFP3, Type IIR, White

Dual-certified filtering half mask offering both FFP3-level respiratory protection and Type IIR medical device functionality. This hypoallergenic mask provides comprehensive protection against solid and liquid aerosols while protecting both the wearer and environment from droplets and fluid splashes. Designed and manufactured in France, it features ultrasonically welded headloops and soft materials for optimal comfort and facial fit.

Product Features:
- FFP3 NR D filtration efficiency
- Type IIR medical device certification
- Ultrasonically welded knitted headloops
- Hypoallergenic and dermatologically tested
- Made in France

Technical Details:
- Protects against solid and liquid aerosols
- Prevents droplet transmission in both directions
- Designed to minimize inward leakage
- Dermatologically tested on 32 subjects by accredited laboratory

Standards:
- EU Regulation 2017/745 on Medical Devices (MD Class I)
- EU Regulation 2016/425 on Personal Protective Equipment (PPE Cat. III)
- CE certified
- Medical mask Type IIR
- FFP3 NR D certified

Recommended Applications:
- Health
- Industry
- Medical

Kolmi Mass Balance Oxygen Mask FFP3, Type IIR, Indiviudally Packed, Size M, White

This dual-certified filtering half mask provides comprehensive protection against solid and liquid aerosols while meeting both medical device and personal protective equipment standards. The mask protects both the wearer from potential body fluid splashes and the environment from wearer-emitted droplets. Featuring ultrasonically welded headloops and soft materials, it ensures optimal comfort and minimal inward leakage while maintaining FFP3 NR D filtration efficiency.

Product Features:
- FFP3 NR D filtration efficiency
- Type IIR medical mask certification
- Ultrasonically welded knitted headloops
- Hypoallergenic and dermatologically tested by accredited laboratory
- Made in France

Technical Details:
- Dual protection: protects wearer and environment
- Designed to minimize inward leakage
- Soft materials for improved face fit

Standards:
- EU Regulation 2017/745 on Medical Devices (MD Class I)
- EU Regulation 2016/425 on Personal Protective Equipment (PPE Cat. III)
- CE certified
- Medical mask Type IIR
- FFP3 NR D certified

Recommended Applications:
- Health
- Industry
- Medical

Kolmi Mass Balance Oxygen Mask FFP3, Type IIR, Indiviudally Packed, Size L, White

This dual-purpose filtering half mask combines FFP3 NR D protection against solid and liquid aerosols with Type IIR medical device certification. It provides bidirectional protection, safeguarding both the wearer from potential body fluid splashes and the environment from user-emitted droplets. Dermatologically tested on 32 people by an accredited laboratory, this French-made mask features ultrasonically welded knitted headloops and hypoallergenic materials for optimal comfort and facial fit.

Product Features:
- FFP3 NR D filtration efficiency
- Type IIR medical certification
- Ultrasonically welded knitted headloops
- Hypoallergenic materials
- Made in France

Technical Details:
- Dual protection against solid and liquid aerosols
- Designed to minimize inward leakage
- Dermatologically tested by accredited laboratory

Recommended Applications:
- Health
- Industry
- Medical

Standards:
- EU Regulation 2017/745 on Medical Devices (MD Class I)
- EU Regulation 2016/425 on Personal Protective Equipment (PPE Cat. III)
- CE certified
- Medical mask Type IIR
- FFP3 NR D certified

WeeSafe WeePro Max Integral Coverall Type 4/5/6, White/Orange

Professional protective coverall offering comprehensive protection against chemical, biological, and particle hazards. This PPE Category III garment features thermosealed seams for protection against fine particles, liquids, and aerosols, while maintaining breathability for user comfort. The antistatic treatment and integrated safety features make it suitable for hazardous environment applications.

Product Features:
- Thermosealed seams for particle, liquid, and aerosol protection
- Antistatic treated material for electrostatic charge dissipation
- Zipper closure with adhesive flap
- Elastic fittings at wrists, ankles, and waist
- Integrated overshoes
- Breathable material construction

Technical Details:
- Protection Types 4, 5, and 6
- Tested against biological risks
- Heat-sealed seam construction

Standards:
- EU Regulation 2016/425 compliant
- PPE Category III certification
- CE certified
- EN 1073-2
- EN 1149-5
- EN 14126

Hopen SafeFeet PP Shoecovers with Plastic Coated Sole, XL

Professional-grade protective shoe covers featuring a dual-layer PP and PE construction with specialized 60µm plasticized soles. These medical-grade covers provide superior slip resistance and extended durability against abrasion on non-smooth floors. The design includes an ankle support elastic band for secure fit and waterproof properties for comprehensive protection.

Product Features:
- Non-slip PE sole construction for enhanced grip
- Waterproof and abrasion-resistant 60µm sole
- Ankle support elastic band for secure fit
- Adaptable to various shoe types and body shapes
- Color coding option for identification

Technical Details:
- PP and PE construction
- Medical Device Class I certification
- CE marked

Recommended Applications:
- Food industry
- Electronics
- Aeronautics
- Laboratory
- Pharmaceutical
- Research
- Nuclear facilities

Standards:
- EU Regulation 2017/745 on Medical Devices
- MD Class I certification

Kolmi Recycled Shoe Cover without Sole, Size XL, White

Environmentally conscious shoe covers featuring hydrophobic spunbond construction made from 90% recycled materials. These protective covers offer universal fit through anatomical design and elastic ankle support, making them suitable for use with or without shoes in medical environments.

Product Features:
- Hydrophobic spunbond from 90% recycled material
- Anatomical shape for versatile fit
- Elastic band for ankle support
- Design without sole

Recommended Applications:
- Medical environments
- Industrial settings
- Hygiene-sensitive areas

Standards:
- EU Regulation 2016/425 compliant
- CE certified
- PPE certified

Hopen SafeFeet PP Shoecovers with Strong Plastic Coated Sole, Size XL, White

Hopen SafeFeet PP Shoecovers with Plastic Coated Sole, Size XL, Green

Hopen SafeFeet PP Shoecovers with Plastic Coated Sole, Size XXL, White

Professional-grade protective shoe covers featuring a polypropylene construction with polyethylene-coated soles. These medical-grade covers incorporate an exclusive anti-slip technology that enhances user safety while providing extended durability against abrasion. The design accommodates various foot morphologies and shoe types, including safety footwear, while offering waterproof protection and ankle support.

Product Features:
- PP construction with PE 60µm plasticized soles
- Anti-slip technology for enhanced traction
- Waterproof and abrasion-resistant design
- Ankle support elastic for secure fit
- Adaptable to various shoe types including safety footwear

Technical Details:
- 60µm non-slip sole thickness
- PP + PE material composition
- Recommended for long-term use

Recommended Applications:
- Food industry
- Electronics
- Aeronautics
- Laboratory
- Pharmaceutical
- Research
- Nuclear facilities

Standards:
- EU Regulation 2017/745 on Medical Devices
- MD Class I certification
- CE marked

Hopen SafeFeet PP Shoecovers with Strong Plastic Coated Sole, Size XL, Blue

Hopen PP Shoecovers with Plastic Coated Sole, Size XXL, White/Blue

Professional-grade protective shoe covers featuring PP spunlaid non-woven material with PE non-slip soles. These overboots are designed to accommodate various foot shapes and shoe types while providing secure coverage through latex-free elastic closures.

Product Features:
- PP spunlaid non-woven construction with PE sole
- Non-slip sole design
- Adaptable fit for various shoe types
- Latex-free elastic closure

Recommended Applications:
- Food industry
- Electronics manufacturing
- Aeronautics
- Laboratory environments
- Pharmaceutical facilities
- Research centers
- Nuclear facilities

MD stands for "Medical Device." It refers to any instruments, apparatus, machines, implants, or other similar or related articles that are intended to be used for human beings for the purpose of diagnosis, prevention, monitoring, treatment or alleviation of disease, injury or disability. In Europe, a MD Label is a special label that must be on all Medical Devices that are sold or used in the European Union (EU). The label must include information about the product, such as the name of the manufacturer, the intended use of the product and CE mark. To be able to sell or use a Medical Device in the EU, the device must meet certain standards and requirements set by the European Union and notified body.

PPE stands for "personal protective equipment." PPE Category 3 refers to equipment that is complex and provide the highest level of protection such as powered respirators, SCBA, and full body suits. In Europe, PPE Category 3 must meet certain safety standards set by the European Union, which means that it must be designed and manufactured to protect the user without causing harm. Companies that make or sell PPE must prove that it meets these standards. They also must have a quality management system in place, have to be audited regularly by a notified body and have to have a technical documentation.

CE Marking is a label that shows a product meets certain safety and environmental standards set by the European Union. To get the CE Marking, a company must test and certify their product meets these standards. CE Marking is required for many products sold in the EU, including electronics, machinery, toys and medical devices. It helps ensure that products are safe for consumers and the environment, and allows for easy trade within the EU.

Dermatologically Tested refers to products that have been tested and proven to be safe for use on the skin. The European Union has regulations for cosmetics products, which includes dermatological testing, to ensure that products are safe for use. To be labeled as dermatologically tested, the product must be tested by a qualified professional, such as a dermatologist, and must not cause any irritation or allergic reactions. The testing must be carried out on a representative sample of human volunteers and the results must be evaluated by a qualified professional before the product can be considered as dermatologically tested and can bear the label. The EU Cosmetics Regulation, lays out the specific requirements for safety assessments and labeling of cosmetics products.

EN 149:2001/AC:2002 is a European standard for filtering half masks for protecting against particles and it is an amendment of EN 149:2001. It outlines additional requirements for mask design and performance testing. The mask must be able to filter a certain percentage of particles and have good breathability. The test results shows how well the mask filters and how easy it is to breathe through. It also specifies the mask's ability to filter out specific airborne particles like dust, mist, and fumes. It includes additional requirements for the performance of the mask, such as the ability to seal against the face and the mask's durability.

EN 149:2001+A1:2009 is a European standard for filtering half masks for protecting against particles and it is an amendment of EN 149:2001. It outlines additional requirements for mask design and performance testing. The mask must be able to filter a certain percentage of particles, have good breathability, and fit securely to the face. The test results shows how well the mask filters and how easy it is to breathe through, also it includes a test for the mask's ability to fit securely to the face. It also specifies the mask's ability to filter out specific airborne particles like dust, mist, and fumes. It includes additional requirements for the performance of the mask, such as the ability to seal against the face and the mask's durability.

EN 149:1991 is a European standard for filtering half masks for protecting against particles. It outlines the requirements for design, performance, and testing of these masks. The mask must be able to filter a certain percentage of particles and have good breathability. The test results shows how well the mask filters and how easy it is to breathe through.

N 149:2001 is a European standard for filtering half masks for protecting against particles. It outlines the requirements for design, performance, and testing of these masks. The mask must be able to filter a certain percentage of particles and have good breathability. The test results shows how well the mask filters and how easy it is to breathe through. It also specifies the mask's ability to filter out specific airborne particles like dust, mist and fumes.

EN 14683:2019 + AC:2019 is a European standard that specifies the performance requirements and test methods for surgical face masks. The standard defines the mask's ability to filter bacteria and particles, as well as its breathability. The mask must also pass tests for flammability, splash resistance, and biocompatibility. The mask must pass all the test to be certified as a surgical mask.

EN 14683:2014 is a European standard that specifies the performance requirements and test methods for cement-based grouts used in pressure pipelines. The standard covers the properties of the grout, including workability, setting time, compressive strength, water permeability, and shrinkage. The standard also includes requirements for testing and inspection during production, as well as acceptance criteria for the final product. Test results must show that the grout meets the standard's performance requirements in order to be considered compliant.

EN 14683:2005 is a European standard that describes the testing methods and performance requirements for face masks, specifically masks that are used to protect against respiratory infections. The tests in this standard include measuring the filtration efficiency, breathability, and resistance to penetration by synthetic blood. The test results must show that the mask has a minimum filtration efficiency of 95% and a maximum breathability of 49 Pa/cm².

EN 14683 is a European standard for face masks. It includes requirements for mask design, testing, and labeling. Test results include things like filtration efficiency and breathability. The standard also includes requirements for packaging and labeling. The 2019 version updates the previous 2014 version.

EN ISO 11737-2:2000 is a standard that defines how to test the sterilization of medical devices. It includes requirements for the methods used to sterilize the device and how to test to make sure the sterilization process was successful. Test results should show that the device is free from harmful microorganisms and safe for use. It was published in 2000

EN ISO 11737-1:2018/A1:2021 is a standard that defines how to test the sterilization of medical devices. It includes requirements for the methods used to sterilize the device and how to test to make sure the sterilization process was successful. Test results should show that the device is free from harmful microorganisms and safe for use. It was amended in 2021 which is why it has A1 at the end of the name.

EN ISO 11737-1:2018 is a standard that tells how to make sure medical devices are cleaned and sterilized properly before they are used on people. It includes rules for the methods used to clean and sterilize the device, and how to test to make sure the cleaning and sterilization process was successful. Test results should show that the device is clean and free from harmful microorganisms.

EN ISO 11737-2:2020 is a standard that defines how to test the sterilization of medical devices. It includes requirements for the methods used to sterilize the device, and how to test to make sure the sterilization process was successful. Test results should show that the device is free from harmful microorganisms and safe for use.

EN ISO 11737-1:2006/AC:2009 is a standard that tells how to make sure medical devices are cleaned and sterilized properly before they are used on people. It includes rules for the methods used to clean and sterilize the device and how to test to make sure the cleaning and sterilization process was successful. Test results should show that the device is clean and free from harmful microorganisms. It was amended in 2009 which is why it has AC at the end of the name.

EN ISO 11737-1:2006 is a standard that tells how to make sure medical devices are cleaned and sterilized properly before they are used on people. It includes rules for the methods used to clean and sterilize the device and how to test to make sure the cleaning and sterilization process was successful. Test results should show that the device is clean and free from harmful microorganisms. It was published in 2006.

EN ISO 11737-2:2009 is a standard that defines how to test the sterilization of medical devices. It includes requirements for the methods used to sterilize the device, and how to test to make sure the sterilization process was successful. Test results should show that the device is free from harmful microorganisms and safe for use. It was published in 2009.

ISO 13485:2016 is a standard that specifies requirements for a quality management system for the design and manufacture of medical devices. It includes requirements for how companies should design, implement, maintain and improve their quality management system to ensure that their medical devices are safe and effective. Test results can include information on how well the quality management system is functioning, how well it is being followed, and how effective it is in preventing defects. The standard also includes requirements for how the company should document and record their quality management system performance and continuously improve it.

The Bacterial Filtration Efficiency (BFE) result for Type IIR in the standard EN 14683:2019 assesses the efficacy of medical face masks in preventing the passage of aerosolized bacteria. This is crucial for medical environments to ensure a high level of protection against potential bacterial infections transmissible through human respiratory droplets. For Type IIR under EN 14683:2019, the bacterial filtration efficiency test involves determining the percentage of bacteria-laden aerosols that do not pass through the mask material. Masks must demonstrate a BFE of ≥98% at a specified bacteria challenge load, ensuring superior filtration capabilities. This higher requirement reflects Type IIR's application in environments where exposure to blood and bodily fluids is possible, granting them suitability for surgeries and other medical proceedings where stringent sterile conditions are essential.

The standard EN 149:2001+A1:2009 designates a classification for filtering half masks, distinguishing between those that are re-usable (R) and non-reusable (NR). When a mask is classified as NR - Not Reusable, as per the result identified for EN 149:2001+A1:2009 NR, it implies that the mask is intended for single use only and should not be used more than once. The test method for determining reusability under this standard involves assessing the mask's material integrity, filter efficiency, and structural stability after simulated use, which might include cleaning, disinfection, and aging procedures. The practical implications of this result are significant; masks labeled as NR must be discarded after one use, highlighting a critical consideration for procurement professionals in terms of inventory, cost management, and usage protocols to ensure safety and compliance.

The EN 149:2001+A1:2009 Dolomite Test, conducted within the framework of EU standards, assesses the resistance of respiratory protective filter masks to clogging by dolomite dust, thus ensuring longer-lasting filter performance under dusty conditions. A result labeled as D in the context of this test indicates that the mask has passed the dolomite dust clogging test and can maintain good breathing resistance over an extended period in a dusty environment, making it suitable for use in high particulate environments. The test method involves exposing the respiratory mask's filter to dolomite dust under controlled conditions and measuring its resistance to clogging (breathing resistance before and after exposure). After successfully passing this test, the mask can be marked with the letter D to signify its performance level, assisting employers or workers in making informed decisions regarding the level of respiratory protection required for specific industrial settings.

EN ISO 9001:2015 is a globally recognized standard that specifies requirements for a quality management system (QMS), focusing on numerous aspects of quality management in organizations, aiming to enhance customer satisfaction through the effective application of the system. The 'Service Reliability' with a 'Passed' designation indicates that an organization has successfully demonstrated its ability to consistently provide services that meet customer and regulatory requirements while aiming for continual improvement. This assessment involves evaluating various elements of the QMS including service planning, execution, and monitoring, to ensure reliability and performance consistency. The practical implications for organizations that pass this aspect of the standard are significant; it establishes them as reliable providers in their industry, enhancing customer trust and satisfaction, and potentially leading to increased business and a competitive advantage.

Medicom SAS, formerly known as Kolmi Hopen, is a prominent French manufacturer specializing in single-use protection products. As part of the global Medicom Group, they have over 50 years of experience in designing and producing innovative solutions for contamination control and risk prevention.
Medicom SAS offers a wide range of products, include Masks and Respirators, Gloves, Protective Clothing including Gowns, coveralls, and head and shoe covers.
Medicom’s products are widely used in medical, dental, clean room and controlled environments as well as industrial, and hygiene sectors, ensuring safety and protection for professionals and patients alike


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