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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CENTRON CORPORATION.Country of Origin
Korea
Authorized Representative
FRISMED HOSLAB INDONESIAAR 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.
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