| Primary Device ID | 07290103039257 |
| NIH Device Record Key | 259ff125-a5ba-4143-b16c-5cb338db11c3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Q-Sense CPM Thermal Sensory Analazer |
| Version Model Number | Q-Sense CPM |
| Catalog Number | MO 00013-CPM |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +97249038800 |
| Info@Medoc-Web.Com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290103039257 [Primary] |
| GS1 | 07290103039752 [Package] Package: Carton [1 Units] In Commercial Distribution |
| LQW | Test, Temperature Discrimination |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 07290103039011 - Medoc Main Station Software | 2023-06-28 Medoc Main Station Base Software |
| 07290103039066 - CoVas | 2023-06-28 CoVAS USB Assy (for TSA-II, Q-Sense and AlgoMed) |
| 07290103039073 - One Button Response Unit | 2023-06-28 |
| 07290103039219 - Thermode CHEPS | 2023-06-28 TSA 2 CHEPS Thermode Standard |
| 07290103039233 - Q-Sense Response Unit | 2023-06-28 Q-Sense PRU (TSA) |
| 07290103039240 - Q-Sense Base Assembly | 2023-06-28 Q-Sense Base Assembly |
| 07290103039264 - Patient Response Unit | 2023-06-28 Patient Unit |
| 07290103039653 - VSA 2 Hand Held | 2023-06-28 VSA 2 Hand Held |