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Cellbind Centrifuge - Indonesia BPOM Medical Device Registration

Cellbind Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209220062. The device is manufactured by HUNAN KECHENG INSTRUMENT EQUIPMENT CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MRK DIAGNOSTICS.

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 : A
Cellbind Centrifuge
Analysis ID: AKL 10209220062

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

MRK DIAGNOSTICS

AR Address

JL. Merpati Mas I Blok B1 NO.46 Perkantoran Tanjung Mas Raya Tanjung Barat

Registration Date

Mar 30, 2022

Expiry Date

Jan 31, 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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DJ Fang

DJ Fang

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