BIOLABO Total and Direct Bilirubin Sulfanilic Acid Method - Indonesia BPOM Medical Device Registration
BIOLABO Total and Direct Bilirubin Sulfanilic Acid Method is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101816841. The device is manufactured by BIOLABO SAS from France, and is classified as Risk Class Kelas Resiko : C. 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
Oct 28, 2022
Expiry Date
Apr 19, 2027
Product Type
Clinical Chemistry Test System
Bilirubin (total or direct) test system
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