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ZILFIX IV - Indonesia BPOM Medical Device Registration

ZILFIX IV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902420619. The device is manufactured by HONY MEDICAL 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 IV
Analysis ID: AKL 10902420619

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

Registration Date

Jun 21, 2024

Expiry Date

Jun 21, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter securement device.

Non Electromedic Sterile

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