| Primary Device ID | 03701505801037 |
| NIH Device Record Key | b69cd0fe-fa26-4b22-b130-dbd77aa2ca0e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | META+ System 1.5cc MV |
| Version Model Number | T040352MV |
| Company DUNS | 764746723 |
| Company Name | TEKNIMED |
| 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 | true |
| 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 | 03701505801037 [Primary] |
| NDN | Cement, Bone, Vertebroplasty |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-04-08 |
| Device Publish Date | 2025-03-31 |
| 03701505801204 - Dynamo | 2026-02-10 |
| 03701505801211 - Dynamo | 2026-02-10 |
| 03701505801228 - Dynamo | 2026-02-10 |
| 03701505801235 - Dynamo | 2026-02-10 |
| 03760177044326 - Signature -x Cement | 2026-02-02 |
| 03760177044333 - Signature -x Cement | 2026-02-02 |
| 03760177044340 - Signature -x Cement | 2026-02-02 |
| 03760177040090 - GENTAFIX | 2025-09-10 |