AGAPPE UREA U.V - Indonesia BPOM Medical Device Registration
AGAPPE UREA U.V is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101615305. The device is manufactured by AGAPPE DIAGNOSTICS SWITZERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AGAPPE DIAGNOSTICS SWITZERLAND GMBH.Country of Origin
Switzerland
Authorized Representative
PT. MULTIMEDILAB KARYAMANDIRIAR Address
GP plaza lantai 3 unit 6, jalan Gelora II No. 01
Registration Date
Jun 10, 2022
Expiry Date
Feb 07, 2027
Product Type
Clinical Chemistry Test System
Urea nitrogen test system (kit & cair)
Invitro Diagnostics
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