MULTIFUGE X4 Pro-MD - Indonesia BPOM Medical Device Registration
MULTIFUGE X4 Pro-MD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209026901. The device is manufactured by THERMO ELECTRON LED GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GENECRAFT LABS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
THERMO ELECTRON LED GMBHCountry of Origin
Germany
Authorized Representative
PT. GENECRAFT LABSAR Address
Business Park kebon Jeruk Blok F2 No 9 Jl. Meruya Ilir Raya No. 88
Registration Date
Dec 21, 2022
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.
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