Primary Device ID | 20643169738335 |
NIH Device Record Key | 4613bc3e-80b6-4390-8d05-6b33291e3c0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DxTerity™ TRA Angio-Kit |
Version Model Number | AKUNIV503 |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Catheter Gauge | 5 French |
Catheter Gauge | 5 French |
Special Storage Condition, Specify | Between 0 and 0 *Store diagnostic catheters in a cool, dry, and dark area. Do not expose diagnostic catheters to UV light |
Special Storage Condition, Specify | Between 0 and 0 *Store diagnostic catheters in a cool, dry, and dark area. Do not expose diagnostic catheters to UV light |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169738331 [Primary] |
GS1 | 20643169738335 [Package] Contains: 00643169738331 Package: PK [5 Units] In Commercial Distribution |
DQO | CATHETER, INTRAVASCULAR, DIAGNOSTIC |
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 | 2017-09-30 |
20643169738380 | CATH AKUNIV604 DXT 6F 5PK ANGIO RAD KIT |
20643169738373 | CATH AKUNIV603 DXT 6F 5PK ANGIO RAD KIT |
20643169738366 | CATH AKUNIV602 DXT 6F 5PK ANGIO RAD KIT |
20643169738359 | CATH AKUNIV601 DXT 6F 5PK ANGIO RAD KIT |
20643169738342 | CATH AKUNIV504 DXT 5F 5PK ANGIO RAD KIT |
20643169738335 | CATH AKUNIV503 DXT 5F 5PK ANGIO RAD KIT |
20643169738328 | CATH AKUNIV502 DXT 5F 5PK ANGIO RAD KIT |
20643169738311 | CATH AKUNIV501 DXT 5F 5PK ANGIO RAD KIT |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DXTERITY 88324666 not registered Live/Pending |
27 Software U.S., Inc. 2019-03-04 |
![]() DXTERITY 87350066 not registered Dead/Abandoned |
DxTerity Diagnostics, Inc. 2017-02-26 |
![]() DXTERITY 87350060 5630340 Live/Registered |
DxTerity Diagnostics, Inc. 2017-02-26 |
![]() DXTERITY 86415894 5392172 Live/Registered |
Medtronic, Inc. 2014-10-06 |