BIOLABO HDL LDL CK-MB CALIBRATOR - Indonesia BPOM Medical Device Registration
BIOLABO HDL LDL CK-MB CALIBRATOR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421247. 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
Jun 28, 2024
Expiry Date
Apr 19, 2027
Product Type
Clinical Chemistry Test System
Calibrator (cair)
Invitro Diagnostics
BIOLABO Control Serum HDL LDL CK-MB Lipids Level 2
BIOLABO Control Serum HDL LDL CK-MB Lipids Level 1
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