FEROZE High-density Lipoprotein Cholesterol Reagent Kit (Direct Method - Selected Suppression Method) - Indonesia BPOM Medical Device Registration
FEROZE High-density Lipoprotein Cholesterol Reagent Kit (Direct Method - Selected Suppression Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421579. The device is manufactured by URIT MEDICAL ELECTRONIC CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BUANA INTIPRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
URIT MEDICAL ELECTRONIC CO., LTDCountry of Origin
China
Authorized Representative
PT. BUANA INTIPRIMA MEDIKAAR Address
Rukan Sentra Niaga Green Lake City Blok F No.3
Registration Date
Aug 19, 2024
Expiry Date
Aug 15, 2027
Product Type
Clinical Chemistry Test System
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