DUMOLAB Salmonella paratyphi BO - Indonesia BPOM Medical Device Registration
DUMOLAB Salmonella paratyphi BO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303520079. The device is manufactured by Dialab Gas. MBH from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LABORA DIAGNOSTIC PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
Dialab Gas. MBHCountry of Origin
Austria
Authorized Representative
PT. LABORA DIAGNOSTIC PARTNERSAR Address
MITRA DIAGNOSTIK LABORA
Registration Date
Feb 01, 2025
Expiry Date
Aug 31, 2026
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
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