ACROSS Gel Forward & Reverse ABO With DVI-/DVI+ - Indonesia BPOM Medical Device Registration
ACROSS Gel Forward & Reverse ABO With DVI-/DVI+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209716883. The device is manufactured by DIAPRO TIBBI URUNLER SAN. VE TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MITRA BAHAGIA CITRA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAPRO TIBBI URUNLER SAN. VE TIC. A.S.Country of Origin
Turkey
Authorized Representative
PT. MITRA BAHAGIA CITRA MEDIKAAR Address
Jl. Raya Kalirungkut 27 Blok C-63
Registration Date
Feb 25, 2024
Expiry Date
Dec 31, 2026
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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