INSIGHT DOA PANEL 6.1 DEVICE - Indonesia BPOM Medical Device Registration
INSIGHT DOA PANEL 6.1 DEVICE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320393. The device is manufactured by TULIP DIAGNOSTICS (P) LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRAVIA CITRA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTICS (P) LTDCountry of Origin
India
Authorized Representative
PT. GRAVIA CITRA LESTARIAR Address
Komplek Rukan Gading Bukit Indah Blok C15 Jl. Bukit Gading Raya
Registration Date
Jun 01, 2023
Expiry Date
Nov 23, 2027
Product Type
Clinical Toxicology Test System
Multi parameter clinical toxicology test system
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DALF IT Salmonella Somatic Antigen OB Paratyphi
DALF IT Salmonella Somatic Antigen OD Typhi
DALF IT Salmonella Somatic Antigen OC Paratyphi
DALF IT Salmonella Flagellar Antigen HC Paratyphi
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