Primary Device ID | 04012030019439 |
NIH Device Record Key | 7c17f39c-424a-4b11-af6e-cf21fe3567ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | seca 232 |
Version Model Number | 232 |
Catalog Number | 2321817008 |
Company DUNS | 316584937 |
Company Name | seca GmbH & Co. KG |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |