VALLEYLAB™ Tungsten Loop Electrodes - Indonesia BPOM Medical Device Registration
VALLEYLAB™ Tungsten Loop Electrodes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603713797. The device is manufactured by BOVIE MEDICAL CORPORATION 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
BOVIE MEDICAL CORPORATIONCountry of Origin
United States
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Dec 30, 2020
Expiry Date
Mar 12, 2025
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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