| Primary Device ID | 03700569625061 |
| NIH Device Record Key | 72da1ac0-bc9d-4a5f-b745-a49e3e7089ef |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | DTDQ1-ST |
| Catalog Number | DTDQ1-ST |
| Company DUNS | 263281904 |
| Company Name | NEWCLIP TECHNICS |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700569625061 [Primary] |
| HRS | Plate, Fixation, Bone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2023-09-18 |
| Device Publish Date | 2017-07-24 |
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