| Primary Device ID | 00880304203624 |
| NIH Device Record Key | 68905e2c-d8a9-45ae-b39c-5b4ef3828e64 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FREEDOM ALL POLY HIP SYSTEM |
| Version Model Number | 11-107125 |
| Catalog Number | 11-107125 |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304203624 [Primary] |
| KWZ | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer |
| 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 |
| 00880304203655 | 11-107128 |
| 00880304203648 | 11-107127 |
| 00880304203631 | 11-107126 |
| 00880304203624 | 11-107125 |
| 00880304203600 | 11-107124 |
| 00880304203594 | 11-107123 |
| 00880304203587 | 11-107122 |