Trima Accel® MultiPlasma Set - Indonesia BPOM Medical Device Registration
Trima Accel® MultiPlasma Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320509. The device is manufactured by TFB MANUFACTURING SRL from Costa Rica, 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
TFB MANUFACTURING SRLCountry of Origin
Costa Rica
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Jun 13, 2023
Expiry Date
Feb 04, 2025
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.
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