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GIMMI Hysteroscopy Sheath - Indonesia BPOM Medical Device Registration

GIMMI Hysteroscopy Sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106320087. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
GIMMI Hysteroscopy Sheath
Analysis ID: AKL 21106320087

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

Oct 25, 2023

Expiry Date

Apr 01, 2028

Product Type

Diagnostic Obstetric and Gynaecological Equipment

Hysteroscope and accessories.

Non Electromedic Non Sterile

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