LABTEST Urea UV - Indonesia BPOM Medical Device Registration
LABTEST Urea UV is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101815441. The device is manufactured by LABTEST DIAGNOSTICA S.A. from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WHIRA PITOE USAHABERSAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LABTEST DIAGNOSTICA S.A.Country of Origin
Brazil
Authorized Representative
PT. WHIRA PITOE USAHABERSAMAAR Address
RUKO BUARAN PERSADA NO. 10, JL. JEND.POL.SOEKAMTO RT.008/06,KEL.DUREN SAWIT
Registration Date
Oct 14, 2020
Expiry Date
Jan 08, 2025
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
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