GETIH Plastic Blood Bag for Single Use ( Triple ) - Indonesia BPOM Medical Device Registration
GETIH Plastic Blood Bag for Single Use ( Triple ) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320754. 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. GETIH SURU INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU LAISHI TRANSFUSION EQUIPMENT CO., LTD.Country of Origin
China
Authorized Representative
PT. GETIH SURU INDONESIAAR Address
JL. Kopral Samiyo 1 No. 23, RT.004/RW.019, Kode Pos 55573, Kel. Sendangtirto, Kec. Berbah, Kab. Sleman, Prov. D.I Yogyakarta
Registration Date
Dec 02, 2023
Expiry Date
May 30, 2026
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
