STEMA Titanium Plate System - Instrument - Indonesia BPOM Medical Device Registration

STEMA Titanium Plate System - Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21303613832. The device is manufactured by STEMA MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EKA GEMILANG MEDIKA.

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BPOM Registered

Risk Class Kelas Resiko : A

STEMA Titanium Plate System - Instrument

Analysis ID: AKL 21303613832

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

STEMA MEDIZINTECHNIK GMBH.

Country of Origin

Germany

Authorized Representative

PT. EKA GEMILANG MEDIKA

AR Address

Ruko BUkit Rivaria Blok A8, Jl. Muchtar RT. 003 RW. 001, Sawangan, Kota Depok - Jawa Barat

Registration Date

Dec 02, 2023

Expiry Date

Jul 11, 2028

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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Kelas Resiko : A

STEMA Titanium Plate System - Instrument - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

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