| Primary Device ID | 04546540399427 |
| NIH Device Record Key | 33032073-5f52-46ef-b302-d9bd00aee61f |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 1791-5110S |
| Catalog Number | 1791-5110S |
| Company DUNS | 330211587 |
| Company Name | Stryker Trauma GmbH |
| 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 | 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 | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Length | 110 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540399427 [Primary] |
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-09-24 |
| 07613327376210 - T2 ALPHA | 2023-12-21 Locking Scalpel |
| 07613327361797 - T2 ALPHA | 2023-06-02 Guide Wire with Ruler Tube |
| 07613327361803 - T2 ALPHA | 2023-06-02 Guide Wire with Ruler Tube |
| 07613327406153 - T2 ALPHA | 2023-06-02 Guide Wire |
| 07613327406184 - T2 ALPHA | 2023-06-02 Guide Wire |
| 07613327095548 - T2 | 2022-05-05 Tibia System Magnetic Trigger |
| 07613153179443 - T2 | 2022-02-08 Locking Screw, Fully Threaded |
| 04546540202475 - T2 | 2022-02-04 Locking Screw, Fully Threaded |