MEDTRONIC SMARTLINK Reusable Instrument - Indonesia BPOM Medical Device Registration
MEDTRONIC SMARTLINK Reusable Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303914956. The device is manufactured by MEDTRONIC SOFAMOR DANEK USA, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDTRONIC SOFAMOR DANEK USA, INC.Country 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 08, 2024
Expiry Date
Feb 06, 2028
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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