FEROZE Lyse - Indonesia BPOM Medical Device Registration
FEROZE Lyse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420354. 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
Nov 11, 2024
Expiry Date
Nov 10, 2027
Product Type
Hematological Reagents
Red cell lysing reagent.
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