Primary Device ID | 20643169486236 |
NIH Device Record Key | d98bef9a-b476-49f7-94d1-ec9dc49d3b33 |
Commercial Distribution Discontinuation | 2017-08-25 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | EOPA CAP™ |
Version Model Number | 77822 |
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 |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Catheter Gauge | 22 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169486232 [Unit of Use] |
GS1 | 20643169486236 [Primary] |
DWF | CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-25 |
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EOPA CAP 78030450 2872461 Live/Registered |
MEDTRONIC, INC. 2000-10-13 |