| Primary Device ID | 00887868061714 |
| NIH Device Record Key | c9592822-ca78-4a7e-a34f-c8ea786fff22 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | A.L.P.S.CANCELLOUS LOCKING SCREW |
| Version Model Number | 8561-55-100 |
| Catalog Number | 856155100 |
| 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 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 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 | 00887868061714 [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 |
| 00887868061714 | 8561-55-100 |
| 00887868061707 | 8561-55-095 |
| 00887868061691 | 8561-55-090 |
| 00887868061684 | 8561-55-085 |
| 00887868061677 | 8561-55-080 |
| 00887868061660 | 8561-55-075 |
| 00887868061653 | 8561-55-070 |
| 00887868061646 | 8561-55-065 |
| 00887868061639 | 8561-55-060 |
| 00887868061622 | 8561-55-055 |
| 00887868061615 | 8561-55-050 |
| 00887868061608 | 8561-55-048 |
| 00887868061592 | 8561-55-046 |
| 00887868061585 | 8561-55-044 |
| 00887868061578 | 8561-55-042 |
| 00887868061561 | 8561-55-040 |
| 00887868061554 | 8561-55-038 |
| 00887868061547 | 8561-55-036 |
| 00887868061530 | 8561-55-034 |
| 00887868061523 | 8561-55-032 |
| 00887868061516 | 8561-55-030 |
| 00887868061509 | 8561-55-028 |
| 00887868061493 | 8561-55-026 |