| Primary Device ID | 00841731106414 |
| NIH Device Record Key | cfb077cc-6c4d-45e0-9aee-9f0f333749e5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cannulated Lesser Hemi Implant |
| Version Model Number | MCHI-13 |
| Company DUNS | 152008371 |
| Company Name | VILEX IN TENNESSEE, 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00841731106414 [Primary] |
| KWD | Prosthesis, Toe, Hemi-, Phalangeal |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
[00841731106414]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-04 |
| 00841731106414 | CHI, Mini 13_Ti Bronze |
| 00841731106407 | CHI, Mini 12_Ti Green |
| 00841731106391 | CHI, Mini 11_Ti Magenta |
| 00841731106384 | CHI, Mini 10_Ti Gold |
| 00841731106377 | CHI, Mini 09_Ti Blue |