| Primary Device ID | 00887868021879 |
| NIH Device Record Key | 8d55401d-13a6-4a7e-ad6d-0d89d0e71727 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VERSANAIL®PROXIMAL HUMERAL LOCKING NAIL KIT |
| Version Model Number | 1818-08-015 |
| Catalog Number | 181808015 |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868021879 [Primary] |
| HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-10-24 |
| 00887868021886 | 1818-10-015 |
| 00887868021879 | 1818-08-015 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VERSANAIL 78080212 2728157 Live/Registered |
BIOMET C.V. 2001-08-20 |