Q-Sense Response Unit AS 00403

GUDID 07290103039233

Q-Sense PRU (TSA)

MEDOC LTD.

Thermotester, diagnostic
Primary Device ID07290103039233
NIH Device Record Key60c41877-34b9-4b6d-b958-4c9a3e786f72
Commercial Distribution StatusIn Commercial Distribution
Brand NameQ-Sense Response Unit
Version Model NumberQ-Sense
Catalog NumberAS 00403
Company DUNS600469191
Company NameMEDOC LTD.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS107290103039233 [Primary]

FDA Product Code

LQWTest, Temperature Discrimination

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-28
Device Publish Date2023-06-20

Devices Manufactured by MEDOC LTD.

07290103039011 - Medoc Main Station Software2023-06-28 Medoc Main Station Base Software
07290103039066 - CoVas2023-06-28 CoVAS USB Assy (for TSA-II, Q-Sense and AlgoMed)
07290103039073 - One Button Response Unit2023-06-28
07290103039219 - Thermode CHEPS2023-06-28 TSA 2 CHEPS Thermode Standard
07290103039233 - Q-Sense Response Unit2023-06-28Q-Sense PRU (TSA)
07290103039233 - Q-Sense Response Unit2023-06-28 Q-Sense PRU (TSA)
07290103039240 - Q-Sense Base Assembly2023-06-28 Q-Sense Base Assembly
07290103039264 - Patient Response Unit2023-06-28 Patient Unit
07290103039653 - VSA 2 Hand Held2023-06-28 VSA 2 Hand Held

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