BIOCROSS Serofuge H-12 - Indonesia BPOM Medical Device Registration
BIOCROSS Serofuge H-12 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209420172. The device is manufactured by CHANGSA YINGTAI INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PANJI PRIMA DINAMIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CHANGSA YINGTAI INSTRUMENT CO., LTDCountry of Origin
China
Authorized Representative
PT. PANJI PRIMA DINAMIKAAR Address
Jalan Kalibata Timur III No. 55 Kalibata, Pancoran
Registration Date
May 09, 2024
Expiry Date
May 07, 2027
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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