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HUIDAMED Surgical Power System (HD-MZI-I) - Indonesia BPOM Medical Device Registration

HUIDAMED Surgical Power System (HD-MZI-I) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002420043. The device is manufactured by CHANGZHOU HUIDA MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is AKSATA MARGA MAKMUR.

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
HUIDAMED Surgical Power System (HD-MZI-I)
Analysis ID: AKL 21002420043

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

AKSATA MARGA MAKMUR

AR Address

Foresta Business Loft 6 Unit 1, BSD City

Registration Date

Mar 22, 2024

Expiry Date

Aug 01, 2027

Product Type

Surgical Neurology Equipment

Powered simple cranial drills, burrs, trephines, and their accessories.

Non Radiation Electromedics

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