LIGASURE ATLAS™ Tissue Fusion - Indonesia BPOM Medical Device Registration
LIGASURE ATLAS™ Tissue Fusion is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603716925. The device is manufactured by COVIDIEN MEDICAL PRODUCTS (SHANGHAI) MANUFACTURING, LLC. from China, 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
Country of Origin
China
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Mar 23, 2021
Expiry Date
Jan 13, 2026
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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