ASNIS 705355S
GUDID 07613327172652
Unthreaded Guide Wire JFX
Stryker Trauma SA
Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile| Primary Device ID | 07613327172652 |
| NIH Device Record Key | 84b29013-8ca4-40d1-ba63-af6d7d9476a0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ASNIS |
| Version Model Number | 705355S |
| Catalog Number | 705355S |
| Company DUNS | 481999654 |
| Company Name | Stryker Trauma SA |
| 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 |
Device Dimensions
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
| Length | 200 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327172652 [Primary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-07-25 |
On-Brand Devices [ASNIS]
| 07613327284539 | Labeling Clip Implants & Instruments JFX |
| 07613327284522 | Screw Rack Lid JFX |
| 07613327284515 | Cannulated Screws Rack JFX |
| 07613327284508 | Labeling Clip General Instruments JFX |
| 07613327284492 | Screw Drawer JFX |
| 07613327284485 | Solid Screws Rack JFX |
| 07613327284478 | Instrument Rack JFX |
| 07613327172867 | Cannulated Screwdriver JFX |
| 07613327172843 | Direct Measuring Gauge JFX |
| 07613327172812 | Positioning Guide JFX |
| 07613327172799 | Sighting Arm |
| 07613327172775 | Double protecting sleeve JFX |
| 07613327172768 | Cannulated Tap JFX |
| 07613327172751 | Cannulated Countersink JFX |
| 07613327172744 | Solid Screw JFX |
| 07613327172737 | Cannulated Countersink JFX |
| 07613327172720 | Cannulated Tap JFX |
| 07613327172706 | Cannulated Countersink JFX |
| 07613327172690 | Cannulated Tap JFX |
| 07613327172683 | Cannulated Drill Bit JFX |
| 07613327172669 | Solid Screw JFX |
| 07613327172652 | Unthreaded Guide Wire JFX |
| 07613327172645 | Unthreaded Guide Wire JFX |
| 07613327172638 | Solid Screw JFX |
| 07613327172614 | Solid Screw JFX |
| 07613327172607 | Solid Screw JFX |
| 07613327172591 | Solid Screw JFX |
| 07613327172577 | Solid Screw JFX |
| 07613327172515 | Solid Screw JFX |
| 07613327172508 | Solid Screw JFX |
| 07613327172478 | Solid Screw JFX |
| 07613327172461 | Solid Screw JFX |
| 07613327172447 | Solid Screw JFX |
| 07613327172430 | Solid Screw JFX |
| 07613327172379 | Solid Screw JFX |
| 07613327172362 | Solid Screw JFX |
| 07613327172355 | Solid Screw JFX |
| 07613327172348 | Solid Screw JFX |
| 07613327172300 | Solid Screw JFX |
| 07613327172287 | Solid Screw JFX |
| 07613327172263 | Solid Screw JFX |
| 07613327172249 | Solid Screw JFX |
| 07613327172232 | Solid Screw JFX |
| 07613327172195 | Solid Screw JFX |
| 07613327172188 | Solid Screw JFX |
| 07613327172164 | Solid Screw JFX |
| 07613327172157 | Solid Screw JFX |
| 07613327172126 | Solid Screw JFX |
| 07613327172119 | Cannulated Screw JFX |
| 07613327172102 | Solid Screw JFX |
Trademark Results [ASNIS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ASNIS 77812391 3802297 Live/Registered |
HOWMEDICA OSTEONICS CORP. 2009-08-25 |
 ASNIS 74425232 not registered Dead/Abandoned |
Howmedica Inc. 1993-08-16 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.