Primary Device ID | 07290103039707 |
NIH Device Record Key | ce287f6c-0d55-4bd1-b7cf-a6c4fe929521 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Q-Sense Thermal Sensory Analazer |
Version Model Number | Q-Sense |
Catalog Number | MO 00013 |
Company DUNS | 600469191 |
Company Name | MEDOC LTD. |
Device Count | 1 |
DM Exempt | false |
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 | false |
OTC Over-The-Counter | false |