AMPLATZER™ Multifenestrated Septal Occluder - Indonesia BPOM Medical Device Registration
AMPLATZER™ Multifenestrated Septal Occluder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503021921. The device is manufactured by ABBOTT MEDICAL from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. NUGRA KARSERA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ABBOTT MEDICALCountry of Origin
United States
Authorized Representative
PT. NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Apr 13, 2020
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Cardiology Equipment
Cardiac occluder
Non Electromedic Sterile
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