Alwide ™ Plus Balloon Catheter - Indonesia BPOM Medical Device Registration
Alwide ™ Plus Balloon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501321082. The device is manufactured by SHANGHAI MICROPORT CARDIOFLOW MEDTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANGHAI MICROPORT CARDIOFLOW MEDTECH CO., LTDCountry of Origin
China
Authorized Representative
UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Oct 18, 2023
Expiry Date
Jul 26, 2028
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Non Sterile
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