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LIND-VAC Clot Activator & Gel Vacuum Blood Collection Tubes - Indonesia BPOM Medical Device Registration

LIND-VAC Clot Activator & Gel Vacuum Blood Collection Tubes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101911857. The device is manufactured by INTERVACTECHNOLOGY OR. from Estonia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAJAWALI NUSINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
LIND-VAC Clot Activator & Gel Vacuum Blood Collection Tubes
Analysis ID: AKL 20101911857

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Estonia

Authorized Representative

PT. RAJAWALI NUSINDO

AR Address

Gedung RNI Jl. Denpasar Raya Kav DIII Kuningan Jakarta Selatan

Registration Date

Apr 11, 2019

Expiry Date

Dec 11, 2023

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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