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 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 |