| Primary Device ID | 20613994887041 |
| NIH Device Record Key | 47ff983b-b9b4-4846-8318-38d6fedbde98 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MC2X® |
| Version Model Number | 91437C |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994887047 [Unit of Use] |
| GS1 | 20613994887041 [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 |
| 00643169560512 | CANN CB91429C MC2X VEN 29/29/29FR 17L |
| 00643169560505 | CANN CB91429 MC2X 29/29/29FR 17L |
| 20643169490158 | CANNULA 91429C MC2X VEN 29FR 10PK 17L |
| 20643169463022 | CANNULA 91429 MC2X 29/29/29FR 10PK 17L |
| 00643169159280 | CANN CB91437C MC2X 29/46/37F17 |
| 00643169159273 | CANN CB91437 MC2X 29/46/37F 17 |
| 00643169159266 | CANN CB91429C MC2X VEN 29/29/29F |
| 00643169159259 | CANN CB91429 MC2X VEN 29/29/29FR |
| 20613994887058 | CANNULA 91437 MC2X 29/37FR 10PK 17L |
| 20613994887041 | CANNULA 91437C MC2X 29/37FR CON 10P 17L |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MC2X 78276546 2878018 Live/Registered |
Medtronic, Inc. 2003-07-21 |