PRESTIGE Monoclonal Anti D Blend - Indonesia BPOM Medical Device Registration
PRESTIGE Monoclonal Anti D Blend is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209022744. The device is manufactured by PRESTIGE DIAGNOSTIC U.K LTD. from United Kingdom, 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
PRESTIGE DIAGNOSTIC U.K LTD.Country of Origin
United Kingdom
Authorized Representative
PT. MITRA BAHAGIA CITRA MEDIKAAR Address
JL.RAYA KALIRUNGKUT 27 BLOK C/63 KALIRUNGKUT
Registration Date
Mar 13, 2024
Expiry Date
Jun 01, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
Invitro Diagnostics
PRESTIGE Diagnostics Salmonella Paratyphi B-O
PRESTIGE Diagnostics Salmonella Paratyphi C-H
PRESTIGE Diagnostics Salmonella Typhi H
PRESTIGE Monoclonal Anti A
PRESTIGE Monoclonal Anti B
PRESTIGE Monoclonal Anti A-B
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