Primary Device ID | 09010522001080 |
NIH Device Record Key | e177b927-194a-4139-9bd7-2254f21ad263 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MEGA ISQ II Instrument |
Version Model Number | Osstell MEGA ISQ II Instrument |
Catalog Number | 100722 |
Company DUNS | 633171269 |
Company Name | Osstell AB |
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 | 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 | true |
OTC Over-The-Counter | false |