GB/T 24787-2009 in English
VALIDSingle-use non-sterile rubber surgical gloves
- Issued on:2009-12-15
- Implemented on:2010-10-01
- File Format:PDF
- Delivery:Within 1 day
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《GB/T 24787-2009一次性使用非灭菌橡胶外科手套》由TC35（全国橡胶与橡胶制品标准化技术委员会）归口，TC35SC4（全国橡胶与橡胶制品标准化技术委员会胶乳制品分会）执行，主管部门为中国石油和化学工业联合会。
本标准规定了一次性使用非灭菌橡胶外科手套的性能、安全性和技术要求。
本标准适用于外科操作中以防止病人和使用者交叉感染的有包装的非灭菌橡胶外科手套。但手套的储存、安全、正确使用、灭菌和随后的处理过程都不适用于本标准。
Introduction
GB/T 24787-2009 Standard Overview
This standard specifies in detail the performance, safety and technical requirements of disposable non-sterile rubber surgical gloves, and is applicable to packaged gloves that prevent cross infection between patients and users during surgical operations.
Classification and Design
| Classification Dimensions | Type Description |
|---|---|
| Material Type | Type 1: Natural rubber latex; Type 2: Neoprene, Styrene-Butadiene Rubber or Thermoplastic Elastomer. |
| Design Type | Straight (R type) and curved (C type), ergonomic. |
| Surface type | Tack surface (T type) and smooth surface (S type). |
| Attachment type | Powdered (P type), powder-free (F type) and coated (C type). |
Standard implementation background and technological evolution
This standard has been converted into a recommended standard since March 2017, replacing the old version and adding a number of technical requirements. The main revisions include:
- Clarify material classification and performance indicators
- Add tensile performance tests before and after aging
- Refine packaging and labeling requirements
Comparison of key performance indicators
| Performance dimensions | Requirements for Type 1 gloves | Requirements for Type 2 gloves |
|---|---|---|
| Tear force before aging (N) | ≥12.5 | ≥9.0 |
| Elongation at break before aging (%) | ≥700 | ≥600 |
| 300% elongation load (N) | ≤2.0 | ≤3.0 |
| Tear force after aging (N) | ≥9.5 | ≥9.0 |
Implementation suggestions
To ensure that the gloves meet the standard requirements, manufacturers should:
- Carry out quality control in strict accordance with the sampling plan (Table 1)
- Select biocompatible materials that comply with GB/T16886
- Establish a complete labeling and packaging management system
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