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NEW BIOSET Vacuum Blood Collection Tube Gel & Clot Activator - Indonesia BPOM Medical Device Registration

NEW BIOSET Vacuum Blood Collection Tube Gel & Clot Activator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221338. The device is manufactured by SHANDONG CHENGWU MEDICAL PRODUCTS FACTORY from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPHARM NUSANTARA BIOMEDICINE.

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BPOM Registered
Risk Class Kelas Resiko : B
NEW BIOSET Vacuum Blood Collection Tube Gel & Clot Activator
Analysis ID: AKL 20101221338

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOPHARM NUSANTARA BIOMEDICINE

AR Address

Jalan Griya Agung Blok O No.72,

Registration Date

Aug 25, 2022

Expiry Date

Aug 23, 2025

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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