Primary Device ID | 20613994878940 |
NIH Device Record Key | 1c65b240-83b8-4791-a99e-aa827b766e58 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Select 3D® II |
Version Model Number | 78520 |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 20 |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00613994878946 [Unit of Use] |
GS1 | 20613994878940 [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 | 2016-06-17 |
00643169159235 | CANN CB78422 SEL 3D II 22F 17L |
00643169158955 | CANN CB78524 SEL 3D II 24F 17L |
00643169158948 | CANN CB78522 SEL 3D II 22F 17L |
00643169158924 | CANN CB78424 SEL 3D II 24F 17L |
20643169486274 | CANNULA 78422 SELECT 3D II 22FR 20PK 17L |
20643169486267 | CANNULA 78420 SELECT 3D II 20FR 20PK 17L |
20613994878971 | CANNULA 78420 SELECT 3D II 20FR 20PK 17L |
20613994878964 | CANNULA 78422 SELECT 3D II 22FR 20PK 17L |
20613994878957 | CANNULA 78424 SELECT 3D II 24FR 20PK 17L |
20613994878940 | CANNULA 78520 SELECT 3D II 20FR 20PK 17L |
20613994878933 | CANNULA 78522 SELECT 3D II 22FR 20PK 10L |
20613994878926 | CANNULA 78524 SELECT 3D II 24FR 20PK 10L |
00763000946869 | CANNULA 78420 SELECT 3D II 20FR 20PK 17L |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SELECT 3D 75606299 2656807 Live/Registered |
Medtronic, Inc. 1998-12-16 |