Primary Device ID | 00889024059542 |
NIH Device Record Key | bc34a916-f680-4e71-a725-0cbe7a27d6f5 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 2359-90-36 |
Catalog Number | 00-2359-090-36 |
Company DUNS | 056038268 |
Company Name | Zimmer, Inc. |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |