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MIZUHO Sugita Titanium Clip and Appliers - Indonesia BPOM Medical Device Registration

MIZUHO Sugita Titanium Clip and Appliers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002220084. The device is manufactured by MIZUHO CORPORATION, GOSEN FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.

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
MIZUHO Sugita Titanium Clip and Appliers
Analysis ID: AKL 21002220084

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. SIGMA KARSA MAGNA

AR Address

Ruko Grosir Cempaka Mas Blok J 38 Jl. Letjend Suprapto

Registration Date

Oct 19, 2022

Expiry Date

Jul 01, 2027

Product Type

Surgical Neurology Equipment

Aneurysm clip applier.

Non Electromedic Non Sterile

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