| Primary Device ID | 00887868005251 |
| NIH Device Record Key | 39cdee4a-a6b0-4ed9-b46c-86422e57e78b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GUIDE WIRE |
| Version Model Number | 1724-28 |
| Catalog Number | 172428 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868005251 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868005251]
Moist Heat or Steam Sterilization
[00887868005251]
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 | 2015-10-24 |
| 00887868005251 | 1724-28 |
| 00887868004001 | 14012-9 |
| 00887868510700 | 8092-22-028 |
| 70887868004000 | 14012-9 |
| 00880304415959 | 945020 |
| 00887868556876 | 909894 |
| 00887868034701 | 8092-32-238 |
| 00887868034695 | 8092-32-228 |
| 00887868034664 | 8092-22-028 |
| 00887868003936 | 1075-38 |
| 00887868003929 | 1075-28 |