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HAIER Biomedical Freezer - Indonesia BPOM Medical Device Registration

HAIER Biomedical Freezer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420196. The device is manufactured by QINGDAO HAIER BIOMEDICAL CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOVALMED.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
HAIER Biomedical Freezer
Analysis ID: AKL 20209420196

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BIOVALMED

AR Address

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

Registration Date

May 30, 2024

Expiry Date

Sep 25, 2025

Product Type

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

Blood storage refrigerator and blood storage freezer.

Non Radiation Electromedics

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