Medical Device Division · registration 240233Active

Medtronic, Inc.

Name: Medtronic, Inc. — Medical Device Division 240233
Creator: Medtronic, Inc.
Keywords: Medtronic, Inc., Medtronic, Inc., 240233, Stents, Vascular, Carotid, Self-Expanding, Medical Device Division

Hong KongStents, Vascular, Carotid, Self-ExpandingClass IVMedtronic, Inc.

Verified

Official record identity

MDACS listing number: 240233
Model name: Protégé RX Self-expanding Carotid Stent System (SEPX-6-20-135, SEPX-6-30-135, SEPX-6-40-135, SEPX-6-60-135, SEPX-7-20-135, SEPX-7-30-135, SEPX-7-40-135, SEPX-7-60-135, SEPX-8-20-135, SEPX-8-30-135, SEPX-8-40-135, SEPX-8-60-135, SEPX-9-20-135, SEPX-9-30-135, SEPX-9-40-135, SEPX-9-60-135, SEPX-10-20-135, SEPX-10-30-135, SEPX-10-40-135, SEPX-10-60-135), Protégé RX Tapered Self-expanding Carotid Stent System (SEPX-8-6-30-135, SEPX-8-6-40-135, SEPX-10-7-30-135, SEPX-10-7-40-135)
Registration date: June 18, 2024
Expiry date: June 17, 2029
Source update date: July 24, 2024
Status: Active

Classification

Risk class: Class IV
Published category: Stents, Vascular, Carotid, Self-Expanding

Published parties

Registrant / registration holder: Medtronic Hong Kong Medical Limited
Manufacturer: Medtronic, Inc.

Official description

Stents, Vascular, Carotid, Self-Expanding

Additional source fields

AMD nomenclature code: 20427
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

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.