Q-Sense Response Unit AS 00403

GUDID 07290103039233

Q-Sense PRU (TSA)

MEDOC LTD.

Thermotester, diagnostic

• Primary Device ID: 07290103039233
• NIH Device Record Key: 60c41877-34b9-4b6d-b958-4c9a3e786f72
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Q-Sense Response Unit
• Version Model Number: Q-Sense
• Catalog Number: AS 00403
• Company DUNS: 600469191
• Company Name: MEDOC LTD.
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290103039233 [Primary]

FDA Product Code

• LQW: Test, Temperature Discrimination

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-28
• Device Publish Date: 2023-06-20

Devices Manufactured by MEDOC LTD.

• 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: 2023-06-28Q-Sense PRU (TSA)
• 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