OCCLUTECH Atrial Flow Regulator Procedure Pack - Indonesia BPOM Medical Device Registration
OCCLUTECH Atrial Flow Regulator Procedure Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503220097. The device is manufactured by OCCLUTECH INTERNATIONAL AB from Sweden, 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
OCCLUTECH INTERNATIONAL ABCountry of Origin
Sweden
Authorized Representative
PT. MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Sep 23, 2022
Expiry Date
Aug 11, 2026
Product Type
Prosthetic Cardiology Equipment
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