Kendall™
GUDID 20763000185811
GW WWTD35001 WHOLEY WIRE V03
Covidien LP
Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device Torque manipulation device| Primary Device ID | 20763000185811 |
| NIH Device Record Key | 20fd0dfc-7935-4b80-8d1b-f647df825afa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Kendall™ |
| Version Model Number | WWTD35001 |
| Company DUNS | 968903703 |
| Company Name | Covidien LP |
| 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 |
Customer Support Contacts
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
Device Dimensions
| 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 |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
| Special Storage Condition, Specify | Between 0 and 0 *Store the device away from sunlight at room temperature in a dry place. |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00763000185817 [Primary] |
| GS1 | 20763000185811 [Package] Contains: 00763000185817 Package: PK [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K120863
FDA Product Code
| DQX | Wire, guide, catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-11-02 |
| Device Publish Date | 2020-10-25 |
On-Brand Devices [Kendall™]
| 00821684058596 | GW WWTD35001 WHOLEY WIRE V02 |
| 20763000185811 | GW WWTD35001 WHOLEY WIRE V03 |
Trademark Results [Kendall]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 KENDALL 90591223 not registered Live/Pending |
SHENZHEN FZONE TECHNOLOGY CO LIMITED 2021-03-19 |
 KENDALL 88660378 not registered Live/Pending |
Bemis Manufacturing Company 2019-10-18 |
 KENDALL 88413516 not registered Live/Pending |
Kendall Jenner, Inc. 2019-05-02 |
 KENDALL 87082661 5292342 Live/Registered |
Phillips 66 Company 2016-06-24 |
 KENDALL 86764949 not registered Dead/Abandoned |
AMERICAN GIRL, LLC 2015-09-22 |
 KENDALL 86584671 5138125 Live/Registered |
Kendall Jenner, Inc. 2015-04-01 |
 KENDALL 86584660 4999443 Live/Registered |
Kendall Jenner, Inc. 2015-04-01 |
 KENDALL 86069210 4587484 Live/Registered |
Covidien LP 2013-09-19 |
 KENDALL 85782377 5027358 Live/Registered |
KPR U.S., LLC 2012-11-19 |
 KENDALL 85401641 not registered Dead/Abandoned |
Abercrombie & Fitch Trading Co. 2011-08-18 |
 KENDALL 85335914 4117666 Live/Registered |
Kendall Electric, Inc. 2011-06-02 |
 KENDALL 85203751 4328702 Live/Registered |
KPR U.S., LLC 2010-12-22 |
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