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STERILIFE Sterilization Gusseted Roll - Indonesia BPOM Medical Device Registration

STERILIFE Sterilization Gusseted Roll is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903420205. The device is manufactured by STERIVIC MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDI KHARISMA INTERNATIONAL.

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
STERILIFE Sterilization Gusseted Roll
Analysis ID: AKL 20903420205

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDI KHARISMA INTERNATIONAL

AR Address

Jl Darmo Kali No. 76

Registration Date

Mar 01, 2024

Expiry Date

Jul 26, 2026

Product Type

General Hospital Equipment and Other Individuals

Sterilization wrap.

Non Electromedic Non Sterile

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