DYNETIC-35 Peripheral Balloon-Expandable Stent - Indonesia BPOM Medical Device Registration
DYNETIC-35 Peripheral Balloon-Expandable Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003127427. The device is manufactured by BIOTRONIK AG from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MULTIDAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOTRONIK AGCountry of Origin
Switzerland
Authorized Representative
MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Dec 01, 2021
Expiry Date
Jun 01, 2026
Product Type
Therapeutic Neurology Equipment
Peripheral Stent
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