Shiley ™ Oral/Nasal Endotracheal Tube Intermediate Cuff Non DEHP - Indonesia BPOM Medical Device Registration
Shiley ™ Oral/Nasal Endotracheal Tube Intermediate Cuff Non DEHP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403221020. The device is manufactured by COVIDIEN from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
COVIDIENCountry of Origin
Mexico
Authorized Representative
PT. MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Jan 25, 2023
Expiry Date
Feb 16, 2027
Product Type
Therapeutic Anesthesia Equipment
Tracheostomy tube and tube cuff.
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