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ISO 13485:2016 Certified Cleanroom Medical Plastic Injection Molding with Full IQ/OQ/PQ Validation

  • ISO 13485:2016 Certified Cleanroom Medical Plastic Injection Molding with Full IQ/OQ/PQ Validation
Lugar de origen Xiamen, Fujian, China
Nombre de la marca Creator
Certificación ISO 9001:2015
Número de modelo KD-MED-001
Cantidad de orden mínima 100 piezas
Precio negotiable
Detalles de empaquetado Cartón de exportación con bolsa de PE, paletizado para envío en contenedor
Tiempo de entrega 25-35 días laborables para molde nuevo, 7-15 días para producción
Condiciones de pago T/T, L/C, PayPal, Western Union
Capacidad de la fuente 100000 piezas por mes
Datos del producto
Certificación ISO 13485:2016 Clase del recinto limpio ISO Clase 8 (100.000)
Validación Protocolo IQ/OQ/PQ
Resaltar

ISO 13485:2016 Certified Medical Plastic Injection Molding

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ISO Class 8 Cleanroom Injection Molding

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Full IQ/OQ/PQ Validation ISO 13485 Molding
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Descripción de producto

ISO 13485 Cleanroom Medical Plastic Injection Molding Service with Full Validation Protocol

Certified to ISO 13485:2016, Xiamen Creator Technology Co., Ltd. provides cleanroom injection molding services for medical device components. Our ISO 13485 quality management system covers the complete product lifecycle from design validation through production, packaging, and sterilization compatibility verification.

Key Features & Advantages

  • ISO 13485:2016 certified quality management system for medical devices
  • Class 100,000 (ISO 8) cleanroom injection molding environment
  • Full IQ/OQ/PQ validation protocol documentation
  • Biocompatibility testing support per ISO 10993 standards
  • Sterilization-compatible material selection (EtO, Gamma, Autoclave)
  • Complete device history records (DHR) for every production lot

Technical Specifications

CertificationISO 13485:2016, ISO 9001:2015
Cleanroom ClassISO Class 8 (100,000)
Mold MaterialS136, NAK80, 420 Stainless Steel
Plastic MaterialMedical-grade PC, ABS, PP, PEEK, PSU, PEI
Mold Precision±0.01mm
Injection Machine80 - 500 ton (dedicated medical line)
ValidationIQ/OQ/PQ Protocol
SterilizationEtO, Gamma, Autoclave compatible

Manufacturing Excellence

Our dedicated medical injection molding workshop features an ISO Class 8 cleanroom with positive pressure, HEPA filtration, and temperature/humidity control. All production personnel follow strict gowning procedures. Our ISO 13485-certified quality system ensures complete traceability from raw material receipt through finished product release, with full validation documentation and device history records maintained for every production lot.

Frequently Asked Questions

Q: Do you have ISO 13485 certification?

A: Yes, we are certified to ISO 13485:2016 for the design and manufacture of medical device components. Our certificate is current and available for review.

Q: What cleanroom class do you operate?

A: We operate an ISO Class 8 (Class 100,000) cleanroom with HEPA filtration, positive pressure, and controlled temperature and humidity.

Q: Can you support sterilization validation?

A: Yes. We work with materials compatible with EtO, Gamma, and Autoclave sterilization. We can coordinate with your sterilization provider for validation testing.

Q: Do you provide full device history records?

A: Absolutely. We maintain complete DHR for every production lot including material certs, process parameters, inspection records, and final release documentation.

Etiquetas:

moldeo a presión de encargo

útiles del moldeo por inyección

servicio que moldea de la inyección