YOFALAB Plastic Blood Bag for Single Use - Indonesia BPOM Medical Device Registration
YOFALAB Plastic Blood Bag for Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209220240. The device is manufactured by SUZHOU LAISHI TRANSFUSION EQUIPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LAKSA MEDIKA INTERNUSA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU LAISHI TRANSFUSION EQUIPMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. LAKSA MEDIKA INTERNUSAAR Address
Pelem Lor No.50 Baturetno
Registration Date
Oct 27, 2022
Expiry Date
Jul 25, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Empty container for the collection and processing of blood and blood components.
Non Electromedic Sterile
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