| Primary Device ID | 00812301020249 |
| NIH Device Record Key | a35950d7-39bd-4a2e-804a-bd033cb20812 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Biomet OrthoPak Non-invasive Bone Growth Stimulator System |
| Version Model Number | 1067719 |
| Catalog Number | 1067719 |
| Company DUNS | 050410323 |
| Company Name | EBI, 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 | 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 | 1.973.299.9300 |
| btbs.csorders@biomet.com | |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812301020249 [Primary] |
| LOF | Stimulator, Bone Growth, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-19 |
| 00812301020355 | ORTHOPAK ASSEMBLY - ROW |
| 00812301020249 | ORTHOPAK STIMULATOR, BIOMET |
| 00812301020232 | ORTHOPAK ASSEMBLY |
| 00887868269318 | 1067718-72 |
| 00887868269301 | 1067718-63 |
| 00887868269295 | 1067718-45 |