BIOLABO ALT/TGP (IFCC) Single Vial - Indonesia BPOM Medical Device Registration
BIOLABO ALT/TGP (IFCC) Single Vial is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101810434. 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 SAS.Country of Origin
France
Authorized Representative
PT. CIPTA VARIA KHARISMA UTAMAAR Address
Jl. Utan Kayu Raya No. 105A Jakarta
Registration Date
Oct 20, 2022
Expiry Date
May 05, 2027
Product Type
Clinical Chemistry Test System
Alanine amino transferase (ALT/SGPT) test system (kit & cair)
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