P4Detect Dengue IgM/IgG - Indonesia BPOM Medical Device Registration
P4Detect Dengue IgM/IgG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321345. The device is manufactured by PRIME4DIA CO.,LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDISINDO BAHANA.
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
PRIME4DIA CO.,LTDCountry of Origin
Korea
Authorized Representative
MEDISINDO BAHANAAR Address
Rukan Graha Cempaka Mas Blok E No.15 Lt.3, Jl. Letjen Suprapto No.1, Jakarta Pusat
Registration Date
Aug 21, 2023
Expiry Date
Oct 04, 2027
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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