TPRI Arterial Cannula - Indonesia BPOM Medical Device Registration
TPRI Arterial Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504124097. The device is manufactured by TIANJIN PLASTICS RESEARCH INSTITUTE, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AURORA MEDIKA GLOBALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TIANJIN PLASTICS RESEARCH INSTITUTE, CO., LTD.Country of Origin
China
Authorized Representative
PT. AURORA MEDIKA GLOBALINDOAR Address
Rukan Aero Bliss Citra 8 Blok C03C No. 8 Citra Garden City
Registration Date
Aug 14, 2023
Expiry Date
Dec 31, 2025
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass vascular catheter, cannula, or tubing.
Non Electromedic Sterile
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