Pure Global

GIMMI AlphaDuoLap 45 L Insufflator - Indonesia BPOM Medical Device Registration

GIMMI AlphaDuoLap 45 L Insufflator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801320699. The device is manufactured by GIMMI GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 : B
GIMMI AlphaDuoLap 45 L Insufflator
Analysis ID: AKL 20801320699

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GIMMI GMBH

Country of Origin

Germany

Authorized Representative

MEGASETIA AMORA KARSA

AR Address

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

Registration Date

Sep 15, 2023

Expiry Date

Apr 01, 2028

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing