XINLE Vacuum Tube K3EDTA - Indonesia BPOM Medical Device Registration
XINLE Vacuum Tube K3EDTA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209911092. The device is manufactured by HEBEI XINLE SCI&TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENDO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HEBEI XINLE SCI&TECH CO., LTD.Country of Origin
China
Authorized Representative
PT. ENDO INDONESIAAR Address
Jl. Raya Menganti 14
Registration Date
Mar 11, 2019
Expiry Date
Dec 31, 2023
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Vacuum-assisted blood collection system.
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