ANGIOPOWER™ Inflation Device - Indonesia BPOM Medical Device Registration
ANGIOPOWER™ Inflation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501710741. The device is manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN REVASS MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD.Country of Origin
China
Authorized Representative
PT. MAIN REVASS MEDIKAAR Address
Jl. Dewi Sartika No. 4B RT 004/007 Kel. Cililitan Kec. Kramat jati
Registration Date
Dec 13, 2023
Expiry Date
Jun 07, 2028
Product Type
Diagnostic Cardiology Equipment
Angiographic injector and syringe.
Non Electromedic Sterile
ANGIOWAY Manifold (Right Off)
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ANGIOWAY Manifold (Right Off)
LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD.