SelectSite™
GUDID 00763000942540
CATHETER C304XL7405 SELECTSITE GLBL MDR
MEDTRONIC, INC.
Vascular guide-catheter, single-use| Primary Device ID | 00763000942540 |
| NIH Device Record Key | fe03c1b9-1992-4a98-85a6-1fcc70541ca7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SelectSite™ |
| Version Model Number | C304XL7405 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Catheter Working Length | 45 Centimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000942540 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K250558
FDA Product Code
| DQY | Catheter, percutaneous |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-07-21 |
| Device Publish Date | 2025-07-13 |
On-Brand Devices [SelectSite™]
| 00613994729798 | CATHETER C304XL7405 SELECTSITE GLOBAL |
| 00613994729781 | CATHETER C304S5906 SELECTSITE GLOBAL |
| 00613994729774 | CATHETER C304L6906 SELECTSITE GLOBAL |
| 00763000147006 | CATHETER C304-HIS US |
| 00763000147013 | CATHETER C304-HIS GLOBAL |
| 00763000942540 | CATHETER C304XL7405 SELECTSITE GLBL MDR |
| 00763000942533 | CATHETER C304L6906 SELECTSITE GLOBAL MDR |
| 00763000942526 | CATHETER C304S5906 SELECTSITE GLOBAL MDR |
Trademark Results [SelectSite]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SELECTSITE 78176921 3165849 Live/Registered |
Medtronic, Inc. 2002-10-22 |
 SELECTSITE 77606354 3714231 Dead/Cancelled |
LTS BUILDERS, LLC 2008-11-03 |
 SELECTSITE 76500843 2810345 Dead/Cancelled |
GENWORTH MORTGAGE HOLDINGS, LLC 2003-03-25 |
 SELECTSITE 76198404 2506842 Live/Registered |
SciQuest.com, Inc. 2001-01-23 |
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