TACTIFLEX ™ Sensor Enabled ™ Ablation Catheter - Indonesia BPOM Medical Device Registration
TACTIFLEX ™ Sensor Enabled ™ Ablation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30501520048. 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
Feb 06, 2025
Expiry Date
Sep 12, 2029
Product Type
Diagnostic Cardiology Equipment
Cardiac ablation percutaneous catheter
Non Electromedic Sterile
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