Kendall™
GUDID 00821684058596
GW WWTD35001 WHOLEY WIRE V02
Covidien LP
Peripheral vascular guidewire extension Peripheral vascular guidewire extension| Primary Device ID | 00821684058596 |
| NIH Device Record Key | 1f18eaf9-6b1d-4710-86fb-8920b357246b |
| 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 |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00821684058596 [Primary] |
| GS1 | 00821684066003 [Package] Package: PK [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K120863
FDA Product Code
| DQY | CATHETER, PERCUTANEOUS |
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 | 2017-06-16 |
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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