AGD Bili-250 - Indonesia BPOM Medical Device Registration
AGD Bili-250 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420006. The device is manufactured by AGD BIOMEDICAL (P) LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTIMEDILAB KARYAMANDIRI.
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
AGD BIOMEDICAL (P) LTD.Country of Origin
India
Authorized Representative
MULTIMEDILAB KARYAMANDIRIAR Address
GP plaza lantai 3 unit 6, jalan Gelora II No. 01
Registration Date
Jan 04, 2024
Expiry Date
Jun 12, 2028
Product Type
Clinical Chemistry Test System
Bilirubin (total and unbound) in the neonate test system (kit & cair)
Invitro Diagnostics
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