BAV Widal S. paratyphi BH - Indonesia BPOM Medical Device Registration
BAV Widal S. paratyphi BH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420302. 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 PT. BAVARIA COMBININDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTICS (P) LTD.Country of Origin
India
Authorized Representative
PT. BAVARIA COMBININDOAR Address
Jl. Ciledug Raya No. 232 Lt. 1 & 2 RT. 008 RW. 001
Registration Date
Jul 05, 2024
Expiry Date
Jul 04, 2027
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,B MONOCLONAL
BAV ANTI-B MONOCLONAL
BAV ANTI-A MONOCLONAL
BAV Widal S. paratyphi AH
BAV Widal S. paratyphi BO
BAV Widal S. paratyphi CO
BAV Widal S. paratyphi AO
BAV Widal S. typhi H
MTD Creatine Kinase MB LS 4+1
MTD DIAGNOSTICS SRL.
MTD Chemistry Control N
MTD DIAGNOSTICS SRL.
HDL DIRECT LS
MTD DIAGNOSTICS SRL.
MTD gGT Sz74 LS 4+1
MTD DIAGNOSTICS SRL.
MTD DIAGNOSTICS BILIRUBIN T LS 2nd GEN 4+1
MTD DIAGNOSTICS SRL.
CHEMISTRY MULTICALIBRATOR
MTD DIAGNOSTICS SRL.
MTD TRIGLYCERIDES GPO-PAP LS Mono
MTD DIAGNOSTICS SRL.
MTD GOT ASAT IFCC LS 4+1
MTD DIAGNOSTICS SRL.
MTD Uric Acid Uricase PAP LS Mono
MTD DIAGNOSTICS SRL.
MTD GLUCOSE GOD-PAP LS Mono
MTD DIAGNOSTICS SRL.