Z-MED ™ Percutaneous Transluminal Valvulopasty Catheter - Indonesia BPOM Medical Device Registration
Z-MED ™ Percutaneous Transluminal Valvulopasty Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320682. The device is manufactured by NUMED INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUGRA KARSERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NUMED INC.Country of Origin
United States
Authorized Representative
PT. NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Nov 11, 2024
Expiry Date
Dec 31, 2028
Product Type
Diagnostic Cardiology Equipment
Balloon aortic valvuloplasty catheter.
Non Electromedic Sterile
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