| Primary Device ID | 00880304373631 |
| NIH Device Record Key | d1825533-065c-443d-a718-1778b2c3b2c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MODULAR PROVISIONAL LINER |
| Version Model Number | 424452 |
| Catalog Number | 424452 |
| 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 | false |
| 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(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 | |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304373631 [Primary] |
| JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
[00880304373631]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-10-28 |
| 00880304373747 | 424469 |
| 00880304373730 | 424468 |
| 00880304373723 | 424467 |
| 00880304373716 | 424464 |
| 00880304373709 | 424463 |
| 00880304373693 | 424462 |
| 00880304373686 | 424461 |
| 00880304373679 | 424460 |
| 00880304373655 | 424454 |
| 00880304373648 | 424453 |
| 00880304373631 | 424452 |
| 00880304373617 | 424448 |
| 00880304373600 | 424447 |
| 00880304373587 | 424445 |