BDI LAB Urea UV Liquid Reagent - Indonesia BPOM Medical Device Registration
BDI LAB Urea UV Liquid Reagent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421662. The device is manufactured by CLINICHEM, LTD. from Hungary, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BERLIANTAMA DIAGNOSTIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLINICHEM, LTD.Country of Origin
Hungary
Authorized Representative
PT. BERLIANTAMA DIAGNOSTIKA INDONESIAAR Address
JL.TAMAN SUNTER INDAH BLOK HJ2 NO.16
Registration Date
Aug 26, 2024
Expiry Date
Aug 25, 2027
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
Invitro Diagnostics
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