FORTRESS Salmonella Paratyphi BO - Indonesia BPOM Medical Device Registration
FORTRESS Salmonella Paratyphi BO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303311818. 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 PT. SETIA GUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FORTRESS DIAGNOSTICS LTD.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
Nov 21, 2023
Expiry Date
Jul 31, 2026
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
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FORTRESS Salmonella Paratyphi CH
FORTRESS Pregnancy Latex Test Kit
TELLGEN Nucleic Acid Extraction Kit
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TELLGEN Lifeready 1000 Automatic Integrated Gene Detection System
HANGZHOU LIFEREAL BIOTECHNOLOGY CO., LTD
FORTRESS Salmonella Paratyphi AO
FORTRESS DIAGNOSTICS LIMITED.
FORTRESS Salmonella Paratyphi BH
FORTRESS DIAGNOSTICS LTD.
FORTRESS Anti Streptolysin O (ASO) Latex Test
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FORTRESS Salmonella Typhi H
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.