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ZILFIX PU - Indonesia BPOM Medical Device Registration

ZILFIX PU is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603420167. The device is manufactured by SHANGHAI CAREUS MEDICAL PRODUCT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
ZILFIX PU
Analysis ID: AKL 11603420167

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MEDI KHARISMA INTERNATIONAL

AR Address

Jl. Darmo kali No.76, RT. 13/RW. 14 Kelurahan Darmo

Registration Date

Jan 20, 2024

Expiry Date

Jun 14, 2026

Product Type

Surgical Equipment

Occlusive wound dressing.

Non Electromedic Non Sterile

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