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CENTRON Blood Collection Mixer and Accessories - Indonesia BPOM Medical Device Registration

CENTRON Blood Collection Mixer and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209025521. The device is manufactured by CENTRON CORPORATION. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 : B
CENTRON Blood Collection Mixer and Accessories
Analysis ID: AKL 20209025521

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

FRISMED HOSLAB INDONESIA

AR Address

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

Registration Date

Nov 02, 2023

Expiry Date

Dec 31, 2026

Product Type

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

Blood mixing devices and blood weighing devices.

Invitro Diagnostics

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