Primary Device ID | 00889024177659 |
NIH Device Record Key | 2ff7acb6-3ea9-4b77-bf00-5fd7a90fbd0d |
Commercial Distribution Discontinuation | 2017-05-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | APR® |
Version Model Number | 9301-00-004 |
Company DUNS | 056038268 |
Company Name | Zimmer, 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 |