Primary Device ID | 04049223104870 |
NIH Device Record Key | 02d7e2e3-4020-429a-8670-60a83d9a7f0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dummy, silver, type COD |
Version Model Number | AGD.A30 |
Catalog Number | AGD.A30 |
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 |