Primary Device ID | 00841036240578 |
NIH Device Record Key | 681b3f2e-0062-4610-905f-6f4eee586634 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WALTERLORENZ™ SURGICAL ASSIST ARM |
Version Model Number | WAL406 |
Catalog Number | WAL406 |
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 | 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(904)741-4400 |
FXJAX-ORDERS@ZIMMERBIOMET.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841036240578 [Primary] |
GAD | RETRACTOR |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841036240578]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-06-25 |
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 |