BAV Widal S.paratyphi "BO' - Indonesia BPOM Medical Device Registration
BAV Widal S.paratyphi "BO' is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303910020. The device is manufactured by TULIP DIAGNOSTICS (P) LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BAVARIA COMBININDO.
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BAV Widal S.paratyphi ‘BO’
Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTICS (P) LTD.Country of Origin
India
Authorized Representative
BAVARIA COMBININDOAR Address
JL. CILEDUG RAYA NO. 232 KEBAYORAN LAMA
Registration Date
Apr 09, 2021
Expiry Date
Jan 12, 2024
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
AIM Malaria Duo Rapid Test (PAN / P. Falciparum)
BAV ANTI-D (Rho) (IgM+IgG) MONOCLONAL
BAV ANTI-A MONOCLONAL
BAV ANTI-B MONOCLONAL
BAV ANTI-A,B MONOCLONAL
BAV Widal S. paratyphi AH
BAV Widal S. paratyphi BH
BAV Widal S. paratyphi BO
BAV Widal S. paratyphi AO
BAV Widal S. paratyphi CO
MTD LDL-DIRECT LS
MTD DIAGNOSTICS SRL.
GPT ALAT IFCC LS 4+1
MTD DIAGNOSTICS SRL.
ITALO M Semi-auto Chemistry Analyzer
MTD DIAGNOSTICS, SRL.
MTD BILIRUBIN D LS 4+1
MTD DIAGNOSTICS, SRL.
BAV Widal S.typhi "O'
TULIP DIAGNOSTICS (P) LTD.