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HAIER Medical Centrifuge LX-60T500-J - Indonesia BPOM Medical Device Registration

HAIER Medical Centrifuge LX-60T500-J is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420237. The device is manufactured by QINGDAO HAIER BIOMEDICAL CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOVALMED.

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BPOM Registered
Risk Class Kelas Resiko : A
HAIER Medical Centrifuge LX-60T500-J
Analysis ID: AKL 10209420237

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. BIOVALMED

AR Address

Plaza Amsterdam Blok B36 RT 003 RW 005 Sentul City, Desa Citaringgul

Registration Date

Jun 28, 2024

Expiry Date

Sep 25, 2025

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Blood bank centrifuge for in vitro diagnostic use.

Invitro Diagnostics

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