BIOLABO AMMONIA ENZYMATIC METHOD - Indonesia BPOM Medical Device Registration
BIOLABO AMMONIA ENZYMATIC METHOD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420782. The device is manufactured by BIOLABO SAS from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CIPTA VARIA KHARISMA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOLABO SASCountry of Origin
France
Authorized Representative
PT. CIPTA VARIA KHARISMA UTAMAAR Address
Jl. Utan Kayu Raya No. 105A Jakarta
Registration Date
Apr 24, 2024
Expiry Date
Apr 19, 2027
Product Type
Clinical Chemistry Test System
Ammonia test system (kit & cair)
Invitro Diagnostics
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