| Primary Device ID | 07613327054507 |
| NIH Device Record Key | 7b660d12-d615-4420-b117-ed6c06f37bbc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FLEXIS |
| Version Model Number | 0682400500 |
| Catalog Number | 0682400500 |
| Company DUNS | 078807493 |
| Company Name | STRYKER COMMUNICATIONS INC. |
| 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 | false |
| 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(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com | |
| Phone | +1(866)726-3705 |
| SCC-CS2@stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327054507 [Primary] |
| FQO | Table, operating-room, ac-powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-15 |
| Device Publish Date | 2023-06-07 |
| 07613327661194 - In-Light Camera | 2025-09-04 |
| 07613327054507 - FLEXIS | 2023-06-15 |
| 07613327054507 - FLEXIS | 2023-06-15 |
| 07613327589344 - OPERON | 2022-03-30 Pad Set 20" Leg, W Cutout, 3" |
| 07613327054286 - NA | 2020-08-06 Suspension, Navigation System, 10' |
| 07613327054293 - NA | 2020-08-06 Suspension, Navigation System |
| 07613327054514 - NA | 2020-08-06 Medium-Duty Dual Yoke |
| 07613327054521 - NA | 2020-08-06 Medium-Duty Suspension |
| 07613327054538 - NA | 2020-08-06 Light-Duty Suspension |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FLEXIS 87671514 not registered Live/Pending |
STYLMARK, INC. 2017-11-03 |
![]() FLEXIS 86577512 4845428 Live/Registered |
KGS Diamond Group S.A. 2015-03-26 |
![]() FLEXIS 85196583 4132737 Live/Registered |
Stryker Corporation 2010-12-13 |
![]() FLEXIS 85019326 4191120 Live/Registered |
CCL LABEL, INC. 2010-04-21 |
![]() FLEXIS 79360055 not registered Live/Pending |
flexis AG 2022-05-04 |
![]() FLEXIS 79253058 5841871 Live/Registered |
CHORDWIZARD SOFTWARE PTY. LIMITED 2018-12-14 |
![]() FLEXIS 78051766 2527643 Live/Registered |
EATON CORPORATION 2001-03-07 |
![]() FLEXIS 76312333 not registered Dead/Abandoned |
flexis AG 2001-09-10 |
![]() FLEXIS 74638266 2014851 Dead/Cancelled |
FERRONATO TECHNOLOGIES GROUP AG 1995-02-23 |
![]() FLEXIS 74047591 1737643 Dead/Cancelled |
UNITED CHAIR COMPANY, INC. 1990-04-10 |
![]() FLEXIS 73740794 1658036 Dead/Cancelled |
SAVOIR 1988-07-15 |
![]() FLEXIS 73617911 1498488 Dead/Cancelled |
KGS DIAMANT AG 1986-09-03 |