| Primary Device ID | 00846832064281 |
| NIH Device Record Key | 5d5f4a51-6540-4933-81fb-7dfb7745daa3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ForeFoot STP |
| Version Model Number | MFT-079C |
| Company DUNS | 968990812 |
| Company Name | TORNIER, INC. |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com | |
| Phone | +1(888)494-7950 |
| customerservice@tornier.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00846832064281 [Primary] |
| HTR | RASP |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
[00846832064281]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-12-07 |
| Device Publish Date | 2015-09-28 |