Pure Global

GIMMI Orthopedic Instruments II - Indonesia BPOM Medical Device Registration

GIMMI Orthopedic Instruments II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420406. The device is manufactured by GIMMI GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGASETIA AMORA KARSA.

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
GIMMI Orthopedic Instruments II
Analysis ID: AKL 11303420406

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

GIMMI GMBH

Country of Origin

Germany

Authorized Representative

PT. MEGASETIA AMORA KARSA

AR Address

JL. PARADISE TIMUR RAYA BLOK F-21 N0. 54

Registration Date

Dec 04, 2024

Expiry Date

Dec 31, 2028

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing