GIMMI Laryngeal Surgical Instruments - Indonesia BPOM Medical Device Registration

GIMMI Laryngeal Surgical Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403420540. 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.

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BPOM Registered

Risk Class Kelas Resiko : A

GIMMI Laryngeal Surgical Instruments

Analysis ID: AKL 10403420540

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

Aug 04, 2024

Expiry Date

Dec 31, 2028

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Electromedic Non Sterile

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GIMMI Laryngeal Surgical Instruments - Indonesia BPOM Medical Device Registration

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Authorized Representative

AR Address

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Expiry Date

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