INBIOS DENV Detect IgM Capture Elisa - Indonesia BPOM Medical Device Registration
INBIOS DENV Detect IgM Capture Elisa is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303719607. The device is manufactured by INBIOS INTERNATIONAL, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRACE ETERNAL MEANS.
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
INBIOS INTERNATIONAL, INC.Country of Origin
United States
Authorized Representative
PT. GRACE ETERNAL MEANSAR Address
Rukan Mutiara Taman Palem A10/17 Cengkareng - Jakarta Barat
Registration Date
Mar 16, 2020
Expiry Date
Jan 28, 2024
Product Type
Serological Reagents
Dengue virus serological reagents
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