Medical Device Division · registration 130267ActiveMedtronic
Hong KongStent/Grafts, Vascular, AortoiliacClass IVMedtronic, Inc.
Official record identity
- MDACS listing number
- 130267
- Model name
- Endurant II Stent Graft System (ETBF2313C124EE, ETBF2313C145EE, ETBF2313C166EE, ETBF2316C124EE, ETBF2316C145EE, ETBF2316C166EE, ETBF2513C124EE, ETBF2513C145EE, ETBF2513C166EE, ETBF2516C124EE, ETBF2516C145EE, ETBF2516C166EE, ETBF2813C124EE, ETBF2813C145EE, ETBF2813C166EE, ETBF2816C124EE, ETBF2816C145EE, ETBF2816C166EE, ETBF2820C124EE, ETBF2820C145EE, ETBF2820C166EE, ETBF3216C124EE, ETBF3216C145EE, ETBF3216C166EE, ETBF3220C124EE, ETBF3220C145EE, ETBF3220C166EE, ETBF3616C145EE, ETBF3616C166EE, ETBF3620C145EE, ETBF3620C166EE, ETLW1610C82EE, ETLW1610C93EE, ETLW1610C124EE, ETLW1610C156EE, ETLW1610C199EE, ETLW1613C82EE, ETLW1613C93EE, ETLW1613C124EE, ETLW1613C156EE, ETLW1613C199EE, ETLW1616C82EE, ETLW1616C93EE, ETLW1616C124EE, ETLW1616C156EE, ETLW1616C199EE, ETLW1620C82EE, ETLW1620C93EE, ETLW1620C124EE, ETLW1620C156EE, ETLW1620C199EE, ETLW1624C82EE, ETLW1624C93EE, ETLW1624C124EE, ETLW1624C156EE, ETLW1624C199EE, ETLW1628C82EE, ETLW1628C93EE, ETLW1628C124EE, ETLW1628C156EE, ETLW1628C199EE, ETEW1010C82EE, ETEW1313C82EE, ETEW2020C82EE, ETEW2424C82EE, ETEW2828C82EE, ETCF2323C49EE, ETCF2525C49EE, ETCF2828C49EE, ETCF3232C49EE, ETCF3636C49EE, ETTF2323C70EE, ETTF2525C70EE, ETTF2828C70EE, ETTF3232C70EE, ETTF3636C70EE, ETUF2314C102EE, ETUF2514C102EE, ETUF2814C102EE, ETUF3214C102EE, ETUF3614C102EE), Endurant IIs Stent Graft System (ESBF2314C103EE, ESBF2514C103EE, ESBF2814C103EE, ESBF3214C103EE, ESBF3614C103EE)
- Registration date
- January 09, 2024
- Expiry date
- August 22, 2028
- Source update date
- March 04, 2024
- Status
- Active
Official value: Valid
Classification
- Risk class
- Class IV
Official value: IV
Published parties
- Registrant / registration holder
- Medtronic Hong Kong Medical Limited
- Manufacturer
- Medtronic, Inc.
Official description
Stent/Grafts, Vascular, Aortoiliac
Additional source fields
- AMD nomenclature code
- 20454
- Traditional Chinese local responsible person
- 美敦力香港醫療有限公司
- Local responsible person phone
- 29191300
- Published manufacturer address
- 710 Medtronic Parkway, Minneapolis, Minnesota 55432, USA
- Revision number
- e
About this record
This page mirrors one official MDACS listing. Roman-numeral classes use Hong Kong’s general medical-device scheme, while letter classes use the IVD scheme. Valid, expired, and delisted records remain distinguishable; no mixed classification scale is fabricated.