| Primary Device ID | 00846832074808 |
| NIH Device Record Key | 0764e9db-de7e-42fc-a923-25d16a7189df |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LATITUDE EV™ |
| Version Model Number | 0030720 |
| Catalog Number | 0030720 |
| Company DUNS | 968990812 |
| Company Name | TORNIER, INC. |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Size Text, specify | 0 |
| Length | 83 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846832074808 [Primary] |
| JDB | PROSTHESIS, ELBOW, SEMI-CONSTRAINED, CEMENTED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-03-25 |
| Device Publish Date | 2020-08-12 |
| 00846832073986 | 9030356 |
| 00846832073979 | 9030351 |
| 00846832073962 | 9030346 |
| 00846832073955 | 9030341 |
| 00846832072965 | 9030398 |
| 00846832072941 | 9030397 |
| 00846832072927 | 9030395 |
| 00846832072590 | 9039005 |
| 00846832072576 | 9039004 |
| 00846832072569 | 9039003 |
| 00846832072552 | 9039002 |
| 00846832072545 | 9039001 |
| 00846832072538 | 9039000 |
| 00846832072521 | 0830825 |
| 00846832072514 | 0830824 |
| 00846832072507 | 0830823 |
| 00846832072491 | 0830822 |
| 00846832072484 | 0830821 |
| 00846832072477 | 0830820 |
| 00846832072460 | 0830819 |
| 00846832072453 | 0830818 |
| 00846832072446 | 0830817 |
| 00846832072439 | 0830816 |
| 00846832074815 | 0030721 |
| 00846832074808 | 0030720 |
| 00846832074754 | 0030711 |
| 00846832074747 | 0030710 |
| 00846832074693 | 0030701 |
| 00846832074686 | 0030700 |