| Primary Device ID | 00880304453395 |
| NIH Device Record Key | 112880b2-c41e-4870-a7e0-d7994184a296 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LACTOSCREW |
| Version Model Number | 905580 |
| Catalog Number | 905580 |
| Company DUNS | 627100159 |
| Company Name | Biomet Sports Medicine, 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304453395 [Primary] |
| MAI | FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-03-21 |
| Device Publish Date | 2015-10-24 |
| 00880304453401 | 905581 |
| 00880304453395 | 905580 |
| 00880304420953 | 905572 |
| 00880304420946 | 905571 |
| 00880304420939 | 905570 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LACTOSCREW 76212866 2753761 Dead/Cancelled |
Biomet Manufacturing Corp. 2001-02-14 |