| Primary Device ID | 05019279495931 |
| NIH Device Record Key | 0c18919c-ae55-4eec-b48c-829411862a0f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AGC PS FEMORAL PROVISIONAL |
| Version Model Number | 32-468024 |
| Catalog Number | 32-468024 |
| Company DUNS | 219322575 |
| Company Name | Biomet Uk Ltd |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com | |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| 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 | 05019279495931 [Primary] |
| HWT | TEMPLATE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
[05019279495931]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-03-22 |
| Device Publish Date | 2020-05-23 |
| 05019279495771 | 32-468012 |
| 05019279495757 | 32-468011 |
| 05019279495979 | 32-468026 |
| 05019279495955 | 32-468025 |
| 05019279495931 | 32-468024 |
| 05019279495917 | 32-468023 |
| 05019279495894 | 32-468022 |
| 05019279495870 | 32-468021 |
| 05019279495856 | 32-468016 |
| 05019279495832 | 32-468015 |
| 05019279495818 | 32-468014 |
| 05019279495795 | 32-468013 |