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SIGMA Sterilization Pouch - Indonesia BPOM Medical Device Registration

SIGMA Sterilization Pouch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903520115. The device is manufactured by BENQ MATERIALS CORPORATION YUNLIN FACTORY 3 from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is QUALTEK CONSULTANT JAKARTA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
SIGMA Sterilization Pouch
Analysis ID: AKL 20903520115

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Feb 01, 2025

Expiry Date

May 15, 2029

Product Type

General Hospital Equipment and Other Individuals

Sterilization wrap.

Non Electromedic Non Sterile

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