ClosureFast™
GUDID 00763000552176
CATHETER CF6-8-100 CLOSUREFAST
MEDTRONIC, INC.
Peripheral vascular electrocautery catheter, single-use| Primary Device ID | 00763000552176 |
| NIH Device Record Key | 6b4790cb-6b7f-4212-a9f3-9ec9d371da5f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ClosureFast™ |
| Version Model Number | CF6-8-100 |
| 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 | false |
| 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 | |
| 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 |
| Device Size Text, specify | 0 |
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Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device in a dry area away from sunlight |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000552176 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K223488
FDA Product Code
| GEI | Electrosurgical, cutting & coagulation & accessories |
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 | 2023-06-26 |
| Device Publish Date | 2023-06-16 |
On-Brand Devices [ClosureFast™]
| 00643169862982 | CATHETER CF7-7-100 CLOSURE FAST V03 |
| 00643169862975 | CATHETER CF7-7-100 CLOSURE FAST V02 |
| 00643169862968 | CATHETER CF7-7-60 CLOSURE FAST V03 |
| 00643169862951 | CATHETER CF7-7-60 CLOSURE FAST V02 |
| 00643169862944 | CATHETER CF7-3-60 CLOSURE FAST V03 |
| 00643169862937 | CATHETER CF7-3-60 CLOSURE FAST V02 |
| 00763000022273 | Catheter CF7-7-60 Closure Fast V04 |
| 00763000552176 | CATHETER CF6-8-100 CLOSUREFAST |
| 00763000552169 | CATHETER CF6-8-60 CLOSUREFAST |
| 00763000702298 | CATHETER CF7-3-60 CLOSURE FAST V05 |
| 00763000702281 | CATHETER CF7-7-60 CLOSURE FAST V05 |
| 00763000702274 | CATHETER CF7-7-100 CLOSURE FAST V05 |
Trademark Results [ClosureFast]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CLOSUREFAST 78981195 3738306 Live/Registered |
COVIDIEN LP 2005-11-15 |
 CLOSUREFAST 78754633 not registered Dead/Abandoned |
VNUS Medical Technologies, Inc. 2005-11-15 |
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