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Disposable medical inspection gloves testingDetection standard GB 7543-2006#GB 7543-2006 Single use sterilized rubber surgical gloves # Single use sterilized rubber surgical gloves # All parameters GB 24788-2009#GB 24788-2009 Medical Gloves Surface Residual Powder, Water Extracted Protein Limit # Medical Gloves # All Items GB 10213-2006#GB 10213-2006 Disposable Medical Rubber Inspection Gloves # Disposable Medical Rubber Inspection Gloves # All Parameters GB 24786-2009# GB 24788-2009#GB 24788-2009 Medical Gloves Surface Residual Powder, Water Extracted Protein Limit # Medical Gloves # All Items GB/T 16886.7-2001#Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residue # Medical devices, medical materials, and drug packaging materials and containers # Determination of dichloroethanol content YY/T 0616-2007#Biological evaluation requirements and tests for disposable medical gloves # Medical devices and drug packaging materials # Cytotoxicity test 
Disposable sterile rubber surgical gloves are classified by category, design, and surface form. It is divided into two material categories: gloves mainly made of natural rubber latex and gloves mainly made of nitrile rubber latex, neoprene latex, styrene butadiene rubber solution, styrene butadiene rubber lotion or thermoplastic elastomer solution. There are two design types: straight and finger bending towards the palm of the hand. There are four surface forms: pitted surface, smooth surface, powdery surface, and powdery surface. Testing items for medical gloves: (1) Sterile medical surgical gloves: They should comply with the requirements of GB 7543-2006 "Disposable sterile rubber surgical gloves", GB 24787-2009 "Disposable non sterile rubber surgical gloves", and GB 24788-2009 "Limit of residual powder and water extracted protein on the surface of medical gloves". （2） Medical examination gloves: They should comply with the requirements of GB 10213-2006 "Disposable Rubber Examination Gloves", GB 24786-2009 "Disposable PVC Medical Examination Gloves", and GB 24788-2009 "Limit of Residual Powder and Water Extracted Protein on the Surface of Medical Gloves". （3） For sterilization using ethylene oxide, the residual amount of ethylene oxide should also comply with the relevant requirements in GB/T 16886.7-2001 "Biological Evaluation of Medical Devices - Part 7: Residual Amount of Ethylene Oxide Sterilization"; If there are endotoxin requirements, they should also comply with the relevant requirements in YY/T 0616-2007 "Biological Evaluation Requirements and Tests for Disposable Medical Gloves" Function of testing report:1. Project bidding: Issue authoritative third-party CMA/CNAS qualification report 2. Online e-commerce platform entry: Quality inspection report recognized by major e-commerce platforms 3. Used as a sales report: issuing legally effective testing reports to make consumers more confident 4. Papers and research: Provide professional personalized testing needs 5. Judicial services: providing scientific, fair, and accurate testing data 6. Industrial problem diagnosis: Verify the troubleshooting and correction of industrial production problems100% inspection and testing process:1. Telephone communication and confirmation of requirements 2. Recommend solutions and confirm quotations 3. Mail samples and arrange testing 4. Progress tracking and result feedback 5. Provide reports and after-sales service 6. If urgent or priority processing is requiredTesting and testing characteristics:1. The testing industry is fully covered, meeting different testing needs 2. Fully cover the laboratory and allocate localized testing nearby3. Engineers provide one-on-one services to make testing more accurate 4. Free initial testing, with no testing fees charged 5. Self service order delivery for free on-site sampling 6. Short cycle, low cost, and attentive service 7. Possess authoritative qualifications such as CMA, CNAS, CAL, etc 8. The testing report is authoritative and effective, and is generally used in China
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