| Primary Device ID | 00887868109591 |
| NIH Device Record Key | 94b13d87-1f65-4ab7-9e7d-d10b2394baa8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DRILL GUIDE |
| Version Model Number | 110008413 |
| Catalog Number | 110008413 |
| 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 | 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 | 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 | 00887868109591 [Primary] |
| HWC | Screw, fixation, bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887868109591]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-11-22 |
| Device Publish Date | 2016-09-26 |
| 00887868109621 | 110008428 |
| 00887868109607 | 110008418 |
| 00887868109591 | 110008413 |
| 00887868073588 | 25-015 |
| 00887868070709 | DG20 |
| 00887868024085 | 2141-07-029 |
| 00887868000621 | 1732 |
| 00887868109614 | 110008423 |
| 00887868447266 | 8162-99-012 |
| 00887868446436 | 8241-64-070 |
| 00887868446382 | 2141-29-400 |
| 00887868448652 | DG20 |
| 00887868463167 | 110008428 |
| 00887868463150 | 110008423 |
| 00887868463143 | 110008418 |
| 00887868463136 | 110008413 |