NSE PTA Balloon Dilatation Catheter - Indonesia BPOM Medical Device Registration
NSE PTA Balloon Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220106. The device is manufactured by GOODMAN CO., LTD. GOODMAN RESEARCH CENTER from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GOODMAN CO., LTD. GOODMAN RESEARCH CENTERCountry of Origin
Japan
Authorized Representative
PT. MAIN WHEEL BEAMAR Address
Perkantoran Duta Merlin Blok C No 58 jalan gajah mada
Registration Date
Mar 16, 2022
Expiry Date
Nov 01, 2026
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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