Select 3D® II
GUDID 20613994878933
CANNULA 78522 SELECT 3D II 22FR 20PK 10L
MEDTRONIC, INC.
Cardiopulmonary bypass cannula, arterial| Primary Device ID | 20613994878933 |
| NIH Device Record Key | d02921ca-c53f-4ca6-af8e-d529df45ed8a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Select 3D® II |
| Version Model Number | 78522 |
| 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 |
Customer Support Contacts
Device Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994878939 [Unit of Use] |
| GS1 | 20613994878933 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K043179
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 | 2016-06-17 |
On-Brand Devices [Select 3D® II]
| 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 |
Trademark Results [Select 3D]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SELECT 3D 75606299 2656807 Live/Registered |
Medtronic, Inc. 1998-12-16 |
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