EDINTRAK 4010
GUDID 07613327363180
System
Stryker Trauma SA
Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use| Primary Device ID | 07613327363180 |
| NIH Device Record Key | 22124d72-226f-4ca1-93f3-cb30da65e5d7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EDINTRAK |
| Version Model Number | 4010 |
| Catalog Number | 4010 |
| Company DUNS | 481999654 |
| Company Name | Stryker Trauma SA |
| 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 | 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327363180 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K940230
FDA Product Code
| HRX | ARTHROSCOPE |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
[07613327363180]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-05-30 |
On-Brand Devices [EDINTRAK]
| 37613327364300 | Hook Blade |
| 07613327364255 | Hook Blade |
| 37613327364232 | Hook Blade |
| 07613327364200 | Hook Blade |
| 07613327363265 | Metatarsal Spreader |
| 07613327363180 | System |
| 07613327363159 | Micro Elevator |
| 07613327362855 | Obturator |
| 07613327362848 | Probe |
| 07613327362831 | System |
| 07613327362770 | Micro Blade Handle |
| 07613327362749 | Cannula |
| 07613327362725 | Sterilization Tray |
| 07613327362688 | Obturator |
| 07613327362602 | Micro Hook Blade |
| 07613327362589 | Cannula |
| 07613327362480 | Angled Micro Hook Blade |
| 37613327362214 | Micro Tip Swabs |
Trademark Results [EDINTRAK]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EDINTRAK 74618042 1986326 Live/Registered |
HOWMEDICA OSTEONICS CORP 1995-01-05 |
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