FORTRESS Salmonella Paratyphi AH - Indonesia BPOM Medical Device Registration
FORTRESS Salmonella Paratyphi AH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303311826. The device is manufactured by FORTRESS DIAGNOSTICS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FORTRESS DIAGNOSTICS LTD.Country of Origin
United Kingdom
Authorized Representative
SETIA GUNA MEDIKAAR Address
KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT
Registration Date
Sep 27, 2024
Expiry Date
Jul 31, 2026
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
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