Pure Global

GIMMI Gynaecology Semi-rigid Instruments - Indonesia BPOM Medical Device Registration

GIMMI Gynaecology Semi-rigid Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103320598. 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 Gynaecology Semi-rigid Instruments
Analysis ID: AKL 11103320598

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

Oct 04, 2023

Expiry Date

Apr 01, 2028

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing