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GB LAB Vacum Blood Collection Tube Heparin - Indonesia BPOM Medical Device Registration

GB LAB Vacum Blood Collection Tube Heparin is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101911152. The device is manufactured by HEBEI XINLE SCI&TECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BERLIANTAMA DIAGNOSTIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GB LAB Vacum Blood Collection Tube Heparin
Analysis ID: AKL 20101911152

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BERLIANTAMA DIAGNOSTIKA INDONESIA

AR Address

JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16

Registration Date

Feb 25, 2022

Expiry Date

Feb 24, 2025

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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