CARDIOBLATE BP2 Ablation Device - Indonesia BPOM Medical Device Registration
CARDIOBLATE BP2 Ablation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603712307. The device is manufactured by CEA MEDICAL MANUFACTURING, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CEA MEDICAL MANUFACTURING, INC.Country of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Sep 28, 2020
Expiry Date
Mar 12, 2025
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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