Pure Global

MIZUHO Endo Neuro Instrument - Indonesia BPOM Medical Device Registration

MIZUHO Endo Neuro Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11002220071. The device is manufactured by MIZUHO CORPORATION, GOSEN FACTORY from Japan, and is classified as Risk Class Kelas Resiko : A. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
MIZUHO Endo Neuro Instrument
Analysis ID: AKL 11002220071

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. SIGMA KARSA MAGNA

AR Address

Ruko Grosir Cempaka Mas Blok J 38 Jl. Letjend Suprapto

Registration Date

Sep 15, 2022

Expiry Date

Jul 01, 2027

Product Type

Surgical Neurology Equipment

Nonpowered neurosurgical instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from MIZUHO CORPORATION, GOSEN FACTORY
Products from the same manufacturer (3 products)