Ansell MicroFlex MK Touch 93-732
Product description
Description
Elevated comfort: These thin, black nitrile medical exam gloves offer enhanced dexterity and tactility in a thin, yet strong design
Black nitrile: Distinctive black color provides contrast while also hiding the appearance of oils, bodily fluids and other stains
ERGOFORM™ Technology: ERGOFORM™ Ergonomic Design Technology reduces muscle strain during repetitive tasks, improving worker comfort and productivity
Optimized grip: Textured on the fingertips for secure handling of instruments and materials
Recommended for
General dentistry
Standard patient examinations
Emergency services
Catering/Meal preparation
General Purpose Auto Aftermarket
Equipment repair and maintenance
Laboratory analysis
Cosmetic Procedures
Tattoo
Product Details
Material: Nitrile
Not Made From Natural Rubber Latex: Yes
Color: Black
Cuff Length: Standard
Powder Content: Powder-Free
External Glove Surface: Textured Fingers
Freedom From Holes (Inspection Level I): 1.5 Aql
Palm Thickness (Mm/Mil): 0.07 / 2.8
Finger Thickness (Mm/Mil): 0.11 / 4.3
Allergy Prevention: Latex (Type I)
Available Sizes: Xs (5.5 - 6), S (6.5 - 7), M (7.5 - 8), L (8.5 - 9), Xl (9.5 - 10), Xxl (10.5 - 11)
Tested For Use With Chemotherapy Drugs: No
Silicone Free: No
Sterile: No
Antistatic: No
Double Gloving Recommendation: Yes, As Underglove
Glove Length (Mm/Inches): 245 / 9.6
Product Segmentation: High Touch
Indicates the statistical quality inspection standard measuring defect rates. Lower AQL values (e.g., 0.65) signify fewer defects and higher protection reliability.
Measurement of material thickness in the palm area, affecting protection level, durability, and dexterity. Critical for matching gloves to specific tasks.
Measures from fingertip to cuff end, determining wrist/forearm coverage. Longer gloves provide enhanced protection against splashes and contaminants.
Measures the material thickness in the finger areas, balancing protection against punctures and chemicals with tactile sensitivity for precision tasks.
Indicates the composition of the gloves, affecting properties like elasticity, chemical resistance, allergen potential, and suitability for specific tasks.
Indicates the glove's pigmentation, which can aid in color-coding tasks, enhancing visibility, or meeting specific industry requirements for contamination control.
Refers to whether gloves have a smooth or textured finish, affecting grip strength, dexterity, and handling ability in wet or dry conditions.
Indicates whether gloves contain donning powder. Powder-free options reduce allergen risks and contamination, while powdered versions offer easier application.
Offers versatile hand protection for various tasks. Balances durability and flexibility, suitable for diverse applications requiring barrier protection.
Provides hand protection with a shorter cuff for greater wrist movement and easy wear. Ideal when full arm coverage isn't required.
Offers complete hand coverage, ensuring hygiene and protection. Ideal for various tasks requiring a barrier against contamination and maintaining cleanliness.
Crafted without natural rubber latex, these gloves are ideal for sensitive skin. Provides a comfortable fit for those with latex sensitivities.
Describes whether fingertips have a smooth or textured surface, affecting grip strength, tactile sensitivity, and handling precision for various applications.
- Chemical Resistance
- Food Service
- Medical Protection
- Antimicrobial Protection
- Radioactive Contamination
- Hand Protection
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Standards and labels
EN ISO 374-1:2016 is a standard that defines the performance requirements for gloves that protect against chemicals and microorganisms. The standard specifies the design, materials, and testing requirements for gloves to protect against chemicals and microorganisms. Possible test results include measurements of the gloves' permeation resistance, degradation, and penetration. It also includes the safety and functionality requirements for gloves.
Test results
Specified Requirements Type BISO 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.
Test results
Medical Management PassedThe ISO 13485:2016 standard is specifically tailored for medical device manufacturers and aims to ensure the quality and safety of medical devices throughout their production and lifecycle. A test result of Passed in the context of the ISO 13485:2016 standard signifies that the medical device manufacturing management system under assessment has successfully met all regulatory and safety requirements stipulated in the standard. This encompasses rigorous evaluations of the manufacturer's quality management system, including processes like risk management, regulatory compliance, and effective process control. The assessment involves auditing processes such as document review, facility inspection, and staff interviews, to verify the adequacy and effectiveness of the quality management system. Meeting the ISO 13485:2016 requirements assists manufacturers in achieving and maintaining regulatory compliance and ensures that their products consistently meet user needs and applicable regulatory standards, which is crucial for entry and continued presence in global markets.
EN 421:1994 is a European standard that specifically focuses on protective gloves designed to provide protection against ionizing radiation and radioactive contamination. The standard outlines requirements and test methods to evaluate the performance of these gloves in terms of their ability to minimize the transfer of radioactive particles and provide a barrier against ionizing radiation. Compliance with EN 421:1994 ensures that the gloves meet established criteria for shielding against radiation and protecting individuals working in environments where ionizing radiation and radioactive contamination are present.
Test results
Radiation & Contamination TestedEN 421:1994 is a European standard that specifies the requirements and test methods for protective gloves designed to protect against ionizing radiation and radioactive contamination. The designation Tested under this standard means that the gloves have undergone evaluations to ensure they can effectively prevent the penetration and permeation of radioactive materials, as well as provide protection against ionizing radiation when used with an appropriate radiation attenuating underglove. The testing involves subjecting the gloves to conditions that simulate exposure to radioactive substances to determine their protective capabilities against both direct radiation and radioactive particles. The practical implications of this result are significant for professionals working in nuclear facilities, medical radiology, and other fields involving radioactive materials. Gloves that are certified as Tested under EN 421:1994 are crucial for maintaining safety standards, preventing radiation burns, and minimizing the risk of radioactive contamination, thereby ensuring the health and safety of individuals in environments with ionizing radiation hazards.
EN ISO 9001:2015 is a standard that sets out the requirements for a quality management system (QMS). It is a set of guidelines that organizations can follow to ensure that they meet customer requirements and enhance customer satisfaction. The standard is based on the plan-do-check-act model and focuses on continuous improvement. It covers the design, development, production, installation, and servicing of products. Organizations can get certified to this standard, which means that they have been independently audited and found to meet the requirements of the standard. The certification process includes regular audits to ensure that the organization continues to meet the standard's requirements.
Test results
Service Reliability PassedEN 374-5:2016 is a European standard for gloves that protect against microorganisms, specifically gloves that are used for medical and dental procedures. It sets rules for how the gloves should protect against microorganisms and how to test if they meet the standards. Gloves that pass the tests can have a label that says they meet the standard. The test results can be pass or fail for each test that checks the gloves resistance to microorganisms.
Test results
Micro-organisms Bacteria & FungiEN 374-5:2016 specifies the requirements and test methods for protective gloves intended to protect against bacteria and fungi. The designation 'Bacteria & Fungi' indicates that the gloves have been tested and verified to provide effective barrier protection against microbial agents. The testing involves evaluating the glove's material and seams for their impermeability to microorganisms under conditions that simulate real-world use, ensuring no penetration occurs through the glove material or at the seams. Gloves certified under this standard are crucial for use in environments such as healthcare, laboratory settings, and any applications where preventing the transmission of infectious agents is essential. They help ensure the safety and hygiene of workers by providing reliable protection against the risks of bacterial and fungal contamination.
Micro-organisms VirusEN 374-5:2016 is a standard that outlines the requirements and testing methods for protective gloves designed to protect against viruses. The designation 'Virus' indicates that the gloves have passed specific tests confirming their barrier effectiveness against viruses. These tests involve assessing the glove material's resistance to penetration by blood-borne pathogens and other virus-containing fluids, using a bacteriophage as a surrogate virus due to its small size and resistance. Gloves that meet this standard are vital in healthcare settings, laboratories, and any environment where there is a risk of exposure to viral infections. They are crucial for preventing the transmission of diseases, ensuring that workers are protected when handling potentially infectious materials, thus enhancing safety and health protocols in workplaces with biological hazards.
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.
Food safe refers to the safety of food products that are used or consumed by people. In Europe, food safety is regulated by the European Union (EU) and the European Food Safety Authority (EFSA). These organizations set standards and requirements for food products to ensure they are safe to eat. To be considered "food safe" in Europe, a product must meet these standards and be free of harmful substances. This includes being free of harmful bacteria, pesticides, and other contaminants. Food products that do not meet these standards cannot be sold or used in the EU.
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.
Ansell delivery terms
Free delivery when you order more than 150,00 € from Ansell
Supplier shipping fee 4,74 €
Brand minimum 1 000,00 €
74,70 €
Price per 10 packages (1 000 pcs)
7,47 € / 100 pcs
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Ansell
Delivery time: 8 business days
Orders from 1 000,00 €
Supplier shipping fee 4,74 €
Free shipping on orders over 150,00 €



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