| Primary Device ID | 00841036242169 |
| NIH Device Record Key | 2e72af81-d389-4376-99ec-6d9c5e9cce5e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WALTERLORENZ™ SURGICAL ASSIST ARM |
| Version Model Number | WAL121 |
| Catalog Number | WAL121 |
| Company DUNS | 046189866 |
| Company Name | BIOMET MICROFIXATION, INC |
| 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 | 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00841036242169 [Primary] |
| PUI | Drape, surgical, exempt |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-06 |
| Device Publish Date | 2019-06-17 |
| 00841036242169 | WAL121 |
| 00841036240790 | WAL409 |
| 00841036240608 | WAL405 |
| 00841036240592 | WAL404 |
| 00841036240585 | WAL407 |
| 00841036240578 | WAL406 |
| 00841036240561 | WAL403 |
| 00841036240554 | WAL402 |
| 00841036240547 | WAL401 |
| 00841036240530 | WAL317 |
| 00841036240523 | WAL316 |
| 00841036240516 | WAL313 |
| 00841036240509 | WAL311 |
| 00841036240493 | WAL310 |
| 00841036240455 | WAL306 |
| 00841036240448 | WAL305 |
| 00841036240431 | WAL304 |
| 00841036240424 | WAL302 |
| 00841036240417 | WAL301 |
| 00841036240400 | WAL119 |
| 00841036240356 | WAL100 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() WALTERLORENZ 87574987 5618521 Live/Registered |
Zimmer Biomet CMF and Thoracic, LLC 2017-08-18 |