AMNOTEC General Container 03 - Indonesia BPOM Medical Device Registration

AMNOTEC General Container 03 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603520320. The device is manufactured by AMNOTEC INTERNATIONAL MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BUMIPA MEDIKA INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

AMNOTEC General Container 03

Analysis ID: AKL 11603520320

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AMNOTEC INTERNATIONAL MEDICAL GMBH

Country of Origin

Germany

Authorized Representative

PT. BUMIPA MEDIKA INDONESIA

AR Address

Ruko Inkopal Blok F 22-23 RT 015 RW 03 Jl. Boulevard Barat Raya

Registration Date

Feb 07, 2025

Expiry Date

Dec 31, 2026

Product Type

General Hospital Equipment and Other Individuals

Sterilization wrap.

Non Electromedic Non Sterile

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AMNOTEC General Container 03 - 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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