| Primary Device ID | 00887868005275 |
| NIH Device Record Key | bf1b7856-95f6-4363-a805-2122ec302556 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AIM™SUPRACONDYLAR NAIL |
| Version Model Number | 1810-20 |
| Catalog Number | 181020 |
| 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 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868005275 [Primary] |
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868005275]
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 |
| 00887868005336 | 1812-30 |
| 00887868005329 | 1812-25 |
| 00887868005312 | 1812-20 |
| 00887868005305 | 1812-15 |
| 00887868005299 | 1810-30 |
| 00887868005282 | 1810-25 |
| 00887868005275 | 1810-20 |
| 00887868005268 | 1810-15 |
| 00887868031434 | 8002-12-030 |
| 00887868031427 | 8002-12-025 |
| 00887868031410 | 8002-12-020 |
| 00887868031403 | 8002-12-015 |
| 00887868031397 | 8002-10-030 |
| 00887868031380 | 8002-10-025 |
| 00887868031373 | 8002-10-020 |
| 00887868031366 | 8002-10-015 |