DALF RD TPHA SPECIFIC TEST - Indonesia BPOM Medical Device Registration
DALF RD TPHA SPECIFIC TEST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321335. The device is manufactured by RAPID LABS LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JAFAREL MEDIATICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RAPID LABS LTDCountry of Origin
United Kingdom
Authorized Representative
PT. JAFAREL MEDIATICSAR Address
Jl. Kendal No. 6A
Registration Date
Aug 15, 2023
Expiry Date
Dec 15, 2027
Product Type
Serological Reagents
Treponema pallidum treponemal test reagents.
Invitro Diagnostics
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AIM Salmonella Antigen O-B
AIM Salmonella Antigen O
AIM Salmonella Antigen O-C
AIM Salmonella Antigen H-C
AIM Salmonella Antigen H
AIM Salmonella Antigen O-A
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