TERUMO Imuflex WB-RP - Indonesia BPOM Medical Device Registration
TERUMO Imuflex WB-RP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320558. The device is manufactured by TERUMO PENPOL PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO PENPOL PRIVATE LIMITEDCountry of Origin
India
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Jul 26, 2023
Expiry Date
Apr 18, 2028
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Empty container for the collection and processing of blood and blood components.
Non Electromedic Sterile
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