MEDTRONIC NUVENT EM Sinus Dilation System - Indonesia BPOM Medical Device Registration
MEDTRONIC NUVENT EM Sinus Dilation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703813193. The device is manufactured by MEDTRONIC XOMED, 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 XOMED, 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
Oct 08, 2024
Expiry Date
Feb 20, 2029
Product Type
Ear, Nose and Throat Surgical Equipment
Ear, nose, and throat manual surgical instrument.
Non Electromedic Sterile
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