| Primary Device ID | 24053613291921 |
| NIH Device Record Key | a09b41f8-20cc-429b-bd7d-ef1eb3b0fce3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Guide Screw |
| Version Model Number | HTD-4P-02-302 |
| Catalog Number | HTD-4P-02-302 |
| Company DUNS | 317409001 |
| Company Name | Gebr. Brasseler GmbH & Co. KG |
| Device Count | 4 |
| 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 | true |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 14053613291924 [Primary] |
| GS1 | 24053613291921 [Package] Contains: 14053613291924 Package: [1 Units] In Commercial Distribution |
| GS1 | 84053613291923 [Unit of Use] |
| HWC | Screw, Fixation, Bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-10-21 |
| Device Publish Date | 2024-10-12 |
| 24053613285951 | Guide Screw Ø 3,20mm |
| 24053613285920 | Guide Screw Ø 3,20mm |
| 24053613292119 | HTZ-2P-035-33 |
| 24053613292034 | HTZ-2P-025-25 |
| 24053613292027 | HTZ-2P-041-00 |
| 24053613292010 | HTZ-2P-040-48 |
| 24053613292003 | HTZ-2P-040-33 |
| 24053613291921 | HTD-4P-02-302 |
| 24053613291914 | HTD-4P-02-303 |