HUMAN Urea LiquiUV - Indonesia BPOM Medical Device Registration
HUMAN Urea LiquiUV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101802644. The device is manufactured by GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SALI POLAPA TOGETHER.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH.Country of Origin
Germany
Authorized Representative
PT. SALI POLAPA TOGETHERAR Address
Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620
Registration Date
Dec 19, 2022
Expiry Date
Nov 08, 2027
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
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