| Primary Device ID | 37613327055697 |
| NIH Device Record Key | 9827a4c0-63c1-4688-84d2-22a50c779d0e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DRI-LOK |
| Version Model Number | 3910075650 |
| Catalog Number | 3910-075-650 |
| Company DUNS | 187502109 |
| Company Name | STRYKER CORPORATION |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Length | 75 Millimeter |
| Outer Diameter | 6.5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327055696 [Primary] |
| GS1 | 37613327055697 [Package] Contains: 07613327055696 Package: pack [5 Units] In Commercial Distribution |
| NBH | Accessories, arthroscopic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-18 |
| Device Publish Date | 2020-08-10 |
| 07613327416558 | Switching Stick, Large |
| 07613327416541 | Switching Stick, Small |
| 07613327061123 | Cannulated Obturator Assembly for Use with 8.0 mm x 75 mm Dri-Lok Cannula Obturator |
| 07613327061116 | Cannulated Obturator Assembly for Use with 6.5 mm x 75 mm Dri-Lok Cannula Obturator |
| 07613327061109 | Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator |
| 07613327061093 | Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator |
| 37613327055802 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055796 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055789 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055772 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055765 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055758 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055741 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055734 | [Non-Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055727 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055710 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055703 | [Non-Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055697 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055680 | [Distal Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055673 | [Non-Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
| 37613327055666 | [Threaded Cannula. Do not resterilize, Do not use if package is damaged] |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DRI-LOK 78405293 2997454 Live/Registered |
Stryker Corporation 2004-04-20 |
![]() DRI-LOK 73298039 1195121 Dead/Cancelled |
Litton Systems, Inc. 1981-02-20 |
![]() DRI-LOK 73152094 1115283 Dead/Cancelled |
PENN-PLAX PLASTICS, INC. 1977-12-14 |
![]() DRI-LOK 72283250 0870556 Live/Registered |
GREEN & GREEN, INC. 1967-10-24 |