| Primary Device ID | 07613327566000 |
| NIH Device Record Key | 16bb9d71-c9e8-49ca-aa53-1b173c846e06 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | T2 ALPHA |
| Version Model Number | 2352-4236S |
| Catalog Number | 2352-4236S |
| 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 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Length | 360 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327566000 [Primary] |
| LXH | Orthopedic manual surgical instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-11 |
| Device Publish Date | 2024-03-01 |
| 07613327566079 | Freehand Drill |
| 07613327566062 | Freehand Drill |
| 07613327566055 | Locking Drill |
| 07613327566024 | Freehand Drill |
| 07613327566017 | Freehand Drill |
| 07613327566000 | Locking Drill |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() T2 ALPHA 87221226 not registered Live/Pending |
Stryker European Holdings I, LLC 2016-10-31 |