LIAISON Progesterone II Genus - Indonesia BPOM Medical Device Registration
LIAISON Progesterone II Genus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101222235. The device is manufactured by DIASORIN INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOMEDIKAL SCIENTIFIC INDONESIA.
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LIAISON Progesteron II Gen
Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASORIN INCCountry of Origin
United States
Authorized Representative
PT. BIOMEDIKAL SCIENTIFIC INDONESIAAR Address
18 Office Park 22nd F1 Suite E, F &G, Jalan TB SIMATUPANG 18
Registration Date
Dec 14, 2022
Expiry Date
May 20, 2026
Product Type
Clinical Chemistry Test System
Progesterone test system (kit & cair)
Invitro Diagnostics
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