CE-lMMUNDIAGNOSTIKA Anti-D Incomplete - Indonesia BPOM Medical Device Registration
CE-lMMUNDIAGNOSTIKA Anti-D Incomplete is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209914848. The device is manufactured by CE-IMMUNDIAGNOSTIKA GMBH, from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CE-IMMUNDIAGNOSTIKA GMBH,Country of Origin
Germany
Authorized Representative
FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Oct 15, 2024
Expiry Date
Jun 07, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
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