Primary Device ID | 04711605574341 |
NIH Device Record Key | 0ae26495-30af-47a3-bd46-6169dfa6dbd2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Femoral component, CR, porous |
Version Model Number | 2103-1135 |
Catalog Number | 2103-1135 |
Company DUNS | 656700556 |
Company Name | UNITED ORTHOPEDIC CORP. |
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 | 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 |
04711605574433 | Femoral component, CR, porous, #6.5, right |
04711605574426 | Femoral component, CR, porous, #5.5, right |
04711605574419 | Femoral component, CR, porous, #4.5, right |
04711605574402 | Femoral component, CR, porous, #3.5, right |
04711605574396 | Femoral component, CR, porous, #2.5, right |
04711605574389 | Femoral component, CR, porous, #1.5, right |
04711605574372 | Femoral component, CR, porous, #6.5, left |
04711605574365 | Femoral component, CR, porous, #5.5, left |
04711605574358 | Femoral component, CR, porous, #4.5, left |
04711605574341 | Femoral component, CR, porous, #3.5, left |
04711605574334 | Femoral component, CR, porous, #2.5, left |
04711605574327 | Femoral component, CR, porous, #1.5, left |