AEX Generator - Indonesia BPOM Medical Device Registration
AEX Generator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603026596. The device is manufactured by SANMINA, HUNTSVILLE, AL from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SANMINA, HUNTSVILLE, ALCountry of Origin
United States
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama
Registration Date
Jan 23, 2025
Expiry Date
Feb 20, 2029
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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