EOPA CAP™
GUDID 20613994888635
CANNULA 77920 EOPA CAP NONVENT 20FR
MEDTRONIC, INC.
Cardiopulmonary bypass cannula, arterial| Primary Device ID | 20613994888635 |
| NIH Device Record Key | 730fdf02-44ab-40a7-a08f-7b591e6dce21 |
| Commercial Distribution Discontinuation | 2017-08-25 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | EOPA CAP™ |
| Version Model Number | 77920 |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 10 |
| 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
Device Dimensions
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
| Catheter Gauge | 20 French |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994888631 [Unit of Use] |
| GS1 | 20613994888635 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K031518
FDA Product Code
| DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-09 |
On-Brand Devices [EOPA CAP™]
| 20643169486236 | CANNULA 77822 EOPA CAP 22FR 10PK 10L |
| 20643169486229 | CANNULA 77820 EOPA CAP 20FR 10PK 10L |
| 20643169486212 | CANNULA 77818 EOPA CAP 18FR 10PK 10L |
| 20613994888642 | CANNULA 77922 EOPA CAP NONVENT 22FR |
| 20613994888635 | CANNULA 77920 EOPA CAP NONVENT 20FR |
| 20613994888628 | CANNULA 77918 EOPA CAP NONVENT 18FR |
Trademark Results [EOPA CAP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EOPA CAP 78030450 2872461 Live/Registered |
MEDTRONIC, INC. 2000-10-13 |
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