Primary Device ID | 04260592020022 |
NIH Device Record Key | 6a12af1e-4bd0-4763-8982-e3cc005d35be |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KAVO LS3 |
Version Model Number | Demo Scanner 0.870.0200 |
Company DUNS | 388004710 |
Company Name | smart optics Sensortechnik GmbH |
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 | false |
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 |