Primary Device ID | 00889024061927 |
NIH Device Record Key | bf3e8802-40d5-447c-9cb6-2acb7d1f4902 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 00-2369-058-35 |
Catalog Number | 00-2369-058-35 |
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 |