EGENS One Step Test Device Dengue IgM/IgG Serum/Plasma Test, Cassette - Indonesia BPOM Medical Device Registration
EGENS One Step Test Device Dengue IgM/IgG Serum/Plasma Test, Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303022106. The device is manufactured by NANTONG EGENS BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SARANA KARYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NANTONG EGENS BIOTECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. SARANA KARYA MEDIKAAR Address
UBUD VILLAGE BLOK KINTAMANI C1 NO.15 KEL.SUDIMARA TIMUR
Registration Date
Jul 14, 2023
Expiry Date
Jun 01, 2028
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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