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CENTRON Centrifuge Balance CB220 - Indonesia BPOM Medical Device Registration

CENTRON Centrifuge Balance CB220 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420097. The device is manufactured by CENTRON CORPORATION from Korea, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.

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
CENTRON Centrifuge Balance CB220
Analysis ID: AKL 10209420097

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Korea

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Mar 19, 2024

Expiry Date

Dec 31, 2026

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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