SBIOCAT AHG GEL - Indonesia BPOM Medical Device Registration
SBIOCAT AHG GEL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220279. The device is manufactured by TULIP DIAGNOSTIC (P) LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIGMA PRIMARY CORE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTIC (P) LTD.Country of Origin
India
Authorized Representative
PT. SIGMA PRIMARY COREAR Address
JL. IR. H. JUANDA RT. 002, RW. 008
Registration Date
Nov 28, 2022
Expiry Date
Mar 20, 2025
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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