ICE*Syphilis - Indonesia BPOM Medical Device Registration
ICE*Syphilis is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220584. The device is manufactured by DIASORIN ITALIA S.P.A UK BRANCH from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASORIN ITALIA S.P.A UK BRANCHCountry of Origin
United Kingdom
Authorized Representative
PT. BIOMEDIKAL SCIENTIFIC INDONESIAAR Address
18 Office Park 22nd F1 Suite E, F &G, Jalan TB SIMATUPANG 18
Registration Date
Aug 21, 2023
Expiry Date
Sep 27, 2027
Product Type
Serological Reagents
Treponema pallidum treponemal test reagents.
Invitro Diagnostics
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LIAISON Murex Anti-HEV IgM
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LIAISON Murex Control Anti-HEV IgM
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LIAISON Murex Anti-HEV IgG
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LIAISON Murex Control Anti-HEV IgG
DIASORIN ITALIA S.P.A.

