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GIMMI Orthopedic Instruments - Indonesia BPOM Medical Device Registration

GIMMI Orthopedic Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420335. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
GIMMI Orthopedic Instruments
Analysis ID: AKL 11303420335

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 09, 2024

Expiry Date

Mar 22, 2028

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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