Primary Device ID | 00194711121021 |
NIH Device Record Key | 873b4ec7-47ef-4c91-ae8b-9c69091924f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Intuy |
Version Model Number | WW-1LK-1W |
Catalog Number | WW-1LK-1W |
Company DUNS | 004280723 |
Company Name | Willowwood Global LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Serial Number | true |
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 | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx | |
Phone | 740-869-3377 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00194711121021 [Primary] |
ISY | Joint, Knee, External Limb Component |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-31 |
Device Publish Date | 2025-03-21 |
00194711121021 | Intuy Knee System (ILK), Silver Color |
00194711121014 | Intuy Knee System (ILK), Black Color |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() INTUY 79392883 not registered Live/Pending |
Reboocon Holding B.V. 2023-08-31 |