SHILEY™ Endobronchial Tube, Left - Indonesia BPOM Medical Device Registration
SHILEY™ Endobronchial Tube, Left is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403022075. The device is manufactured by COVIDIEN FORMERLY MALLINCKRODT MEDICAL CORNAMADDY from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Ireland
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 31, 2024
Expiry Date
Feb 20, 2029
Product Type
Therapeutic Anesthesia Equipment
Bronchial tube.
Non Electromedic Sterile
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SHILEY™ Adult Flexible EVAC Tracheostomy Tube with TaperGuard Cuff, Single Cannula (No Inner Cannula)
SHILEY Adult Flexible EVAC Tracheostomy Tube with TaperGuard Cuff, Reusable Inner Cannula (RIC}
SHILEY™ Endobronchial Tube Right
Shiley Endobronchial Tube Left with Carinal Hook
SHILEY™ Endobronchial Tube Left with Carinal Hook
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