LIGASURE Maryland Jaw Laparoscopic Sealer/Dividers - Indonesia BPOM Medical Device Registration
LIGASURE Maryland Jaw Laparoscopic Sealer/Dividers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603813347. The device is manufactured by COVIDIEN 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
COVIDIENCountry of Origin
United States
Authorized Representative
PT. 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
May 16, 2023
Expiry Date
Feb 16, 2027
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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