| Primary Device ID | 00887868343681 |
| NIH Device Record Key | 5e17c745-e382-4bf7-b44c-9a5a06728017 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Prelude® PF |
| Version Model Number | 110018152 |
| Catalog Number | 110018152 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868343681 [Primary] |
| KRR | PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-10-21 |
| Device Publish Date | 2019-10-11 |
| 00887868343735 | 110018164 |
| 00887868343728 | 110018156 |
| 00887868343711 | 110018155 |
| 00887868343704 | 110018154 |
| 00887868343698 | 110018153 |
| 00887868343681 | 110018152 |
| 00887868343674 | 110018151 |
| 00887868343667 | 110018150 |
| 00887868343650 | 110018149 |
| 00887868343643 | 110018148 |
| 00887868343636 | 110005120 |
| 00887868343629 | 110005119 |
| 00887868343612 | 110005118 |
| 00887868343605 | 110005117 |
| 00887868343599 | 110005116 |
| 00887868343582 | 110005115 |
| 00887868343575 | 110004335 |
| 00887868343568 | 110004334 |
| 00887868343551 | 110004333 |
| 00887868343544 | 110004332 |
| 00887868343537 | 110004331 |
| 00887868343520 | 110004330 |
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