| Primary Device ID | 00840420127174 |
| NIH Device Record Key | e0bd8497-4036-4f03-aa38-0101cb7a988e |
| Commercial Distribution Discontinuation | 2016-01-27 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | CROSSCHECK |
| Version Model Number | CCP-UTN5 |
| Company DUNS | 807201207 |
| Company Name | WRIGHT MEDICAL TECHNOLOGY, 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 | true |
| 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 |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840420127174 [Primary] |
| HRS | Plate, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00840420127174]
Moist Heat or Steam Sterilization
[00840420127174]
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 | 2015-12-16 |