GLENBIO Creatinine Jaffe Reagent Kit - Indonesia BPOM Medical Device Registration
GLENBIO Creatinine Jaffe Reagent Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221458. The device is manufactured by GLENBIO LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARDIKHA UMRAN ABADI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GLENBIO LTDCountry of Origin
United Kingdom
Authorized Representative
PT. ARDIKHA UMRAN ABADIAR Address
Jl. Bintara VIII Nomor 100 A
Registration Date
Sep 12, 2022
Expiry Date
Jan 03, 2027
Product Type
Clinical Chemistry Test System
Creatine test system (kit & cair)
Invitro Diagnostics
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