LigaSure ™ XP Maryland Jaw Sealer/Divider - Indonesia BPOM Medical Device Registration
LigaSure ™ XP Maryland Jaw Sealer/Divider is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420488. The device is manufactured by COVIDIEN 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
COVIDIENCountry 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
Mar 01, 2024
Expiry Date
Feb 28, 2028
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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