FORTRESS Salmonella Typhi H - Indonesia BPOM Medical Device Registration
FORTRESS Salmonella Typhi H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303311884. The device is manufactured by FORTRESS DIAGNOSTICS LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FORTRESS DIAGNOSTICS LIMITED.Country of Origin
United Kingdom
Authorized Representative
PT. SETIA GUNA MEDIKAAR Address
KOMPLEK TAMAN KEBUN JERUK BLOK AA IV NO. 39-40, KEBUN JERUK, JAKARTA BARAT
Registration Date
Sep 13, 2024
Expiry Date
Jul 31, 2026
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
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TELLGEN Lifeready 1000 Automatic Integrated Gene Detection System
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FORTRESS Salmonella Paratyphi AO
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FORTRESS Salmonella Paratyphi BH
FORTRESS DIAGNOSTICS LTD.
FORTRESS Anti Streptolysin O (ASO) Latex Test
FORTRESS DIAGNOSTICS LIMITED.
FlowPRA™ Negative Control
ONE LAMBDA INC
FORTRESS ANTI - D IgG/IgM Blend
FORTRESS DIAGNOSTICS LIMITED.
FORTRESS Anti - B Monoclonal
FORTRESS DIAGNOSTICS LTD
FlowPRA ™ Class I Positive Control
ONE LAMBDA INC.
FlowPRA™ Class II Positive Control
ONE LAMBDA INC.