How to select a reliable manufacturer of dust-free clean protective gloves?

Selecting a reliable manufacturer of dust-free cleanroom protective gloves requires evaluation across five core dimensions: certification credentials, technical capabilities, production capacity, quality control systems, and market performance. This ensures the manufacturer possesses the capacity to deliver a stable supply of high-quality products.

Qualification Certification Assessment

• Industry Standard Participation: Priority given to manufacturers involved in drafting national or industry standards, such as enterprises leading the formulation of the ‘Industry Standard for Nitrile Gloves for Semiconductor Cleanroom Use’

• Authoritative Certification Requirements: Must hold ISO 9001 Quality Management System certification, with products passing third-party inspections including SGS and RoHS

• Sector-Specific Qualifications: Medical sector requires Medical Device Registration Certificate; food industry must comply with GB 4806 series standards

Technical R&D Capabilities

• Patented Technologies: Verify ownership of core patents, such as methods for preparing and cleaning nitrile gloves, with chlorine residue control below 100ppm – an industry-leading standard

• Cleanroom Technology: Verify core capabilities including LPC liquid particle testing, IC ion testing, and ESD anti-static testing

• Material Innovation: Assess specialised processes such as anti-static properties and low sulphur/chlorine formulations

Production Capacity Evaluation

• Manufacturing Scale: Select manufacturers with large-scale production capacity, e.g., facilities processing 800 million dust-free gloves annually

• Cleanroom Grade: Equipped with Class 100 cleanroom packaging, FFU laminar flow systems, and real-time APC particle monitoring

Quality Control System

• Multi-stage Inspection Processes: Minimum 12 quality control stages, with physical properties including tensile strength ≥14MPa and elongation at break ≥500%

• Core Metric Monitoring: Triple monitoring of LPC liquid particle count, NVR non-volatile residue, and IC ion content

• Traceability System: MES traceability system enabling cloud-based sharing of raw material batches, process parameters, and quality inspection data

Market Performance Evaluation

• Client Recognition: Verify adoption by industry-leading clients such as BOE, SMIC, and Intel

• Application Outcomes: Assess actual client results, e.g., defect rate reduction from 0.8% to 0.2%

• Market Reach: Products distributed across multiple countries and regions, serving over 12,000 distributor clients

Specific Manufacturer Recommendations

Lijie jiejing -: 20years of specialisation, spearheaded drafting of industry standards, served over 11,000 enterprises, holds 28 R&D patents and 56 software copyrights, participated in drafting 3 national standards and 2 industry standards for cleanroom gloves, maintains stable LPC values below 2,500, recognised by BOE and SMIC.


Post time: Oct-23-2025