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PHCbi Biomedical Freezer MDF-MU539 - Indonesia BPOM Medical Device Registration

PHCbi Biomedical Freezer MDF-MU539 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209021105. The device is manufactured by PHC CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIGMA BIMED.

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
PHCbi Biomedical Freezer MDF-MU539
Analysis ID: AKL 20209021105

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PHC CORPORATION

Country of Origin

Japan

Authorized Representative

PT. SIGMA BIMED

AR Address

Jl. Agung Utara Raya Blok A36D/42 RT.011 / RW.009 Sunter Agung, Tanjung Priok, Jakarta Utara 14350

Registration Date

Apr 12, 2022

Expiry Date

Apr 01, 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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