FORTRESS Serological Albumin 22 % - Indonesia BPOM Medical Device Registration
FORTRESS Serological Albumin 22 % is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209312930. The device is manufactured by FORTRESS DIAGNOSTICS LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FORTRESS DIAGNOSTICS LIMITEDCountry of Origin
United Kingdom
Authorized Representative
PT. SETIA GUNA MEDIKAAR Address
KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT
Registration Date
Nov 23, 2021
Expiry Date
Jan 01, 2026
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood group substances of nonhuman origin for in vitro diagnostic use.
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