YINGTAI Medical Centrifuge - Indonesia BPOM Medical Device Registration
YINGTAI Medical Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209915852. The device is manufactured by CHANGSHA YINGTAI INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HARMONI PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CHANGSHA YINGTAI INSTRUMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. HARMONI PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Sep 09, 2019
Expiry Date
Mar 21, 2024
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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