TERUMO Automatic Component Extractor T-ACE II+ and - Indonesia BPOM Medical Device Registration
TERUMO Automatic Component Extractor T-ACE II+ and is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209111412. The device is manufactured by TERUMO BCT EUROPE N.V. from Belgium, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO BCT EUROPE N.V.Country of Origin
Belgium
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Dec 16, 2020
Expiry Date
Nov 17, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
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