Primary Device ID | 04049223104788 |
NIH Device Record Key | e3144254-3583-4d50-9b32-ec9b9401da7a |
Commercial Distribution Discontinuation | 2020-06-30 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Dummy, silver, type CCZ |
Version Model Number | AGD.A21 |
Catalog Number | AGD.A21 |
Company DUNS | 331080432 |
Company Name | Eckert & Ziegler BEBIG GmbH |
Device Count | 1 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
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 |