AXP II Device System - Indonesia BPOM Medical Device Registration
AXP II Device System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320727. The device is manufactured by THERMOGENESIS CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOMED GLOBAL SINERGI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
THERMOGENESIS CORPORATIONCountry of Origin
United States
Authorized Representative
PT. BIOMED GLOBAL SINERGIAR Address
BIOMED GLOBAL SINERGI
Registration Date
Dec 27, 2023
Expiry Date
Sep 20, 2028
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Cord blood processing system and storage container
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