Primary Device ID | 04012030018951 |
NIH Device Record Key | f6edb3b0-ebba-4b51-bcab-ef86c975ba96 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | seca 769 |
Version Model Number | 769 |
Catalog Number | 7691321998 |
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 |