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GBLAB Specimen Container - Indonesia BPOM Medical Device Registration

GBLAB Specimen Container is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101917072. The device is manufactured by NINGBO MFLAB MEDICAL INSTRUMENT.CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BERLIANTAMA DIAGNOSTIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
GBLAB Specimen Container
Analysis ID: AKL 20101917072

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. BERLIANTAMA DIAGNOSTIKA INDONESIA

AR Address

JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16

Registration Date

Oct 10, 2022

Expiry Date

Oct 10, 2025

Product Type

Pathology Equipment and Accessories

Specimen transport and storage container.

Invitro Diagnostics

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DJ Fang

DJ Fang

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