Pulsar - 18 Peripheral Self Expanding Nitinol Stent System - Indonesia BPOM Medical Device Registration
Pulsar - 18 Peripheral Self Expanding Nitinol Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503511079. The device is manufactured by BIOTRONIK AG from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOTRONIK AGCountry of Origin
Switzerland
Authorized Representative
PT. MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Nov 06, 2019
Expiry Date
Apr 01, 2024
Product Type
Prosthetic Cardiology Equipment
Coronary stent
Non Electromedic Sterile
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