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CVS Pharmacy

FDA UDI

Class II (US FDA UDI)

by Woonsocket Prescription Center, Incorporated

Identity

Trade Name
CVS Pharmacy FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
Non Contact Infrared Body Thermometer designed to be used for intermittent measurement and monitoring of human bod temperature by consumers in the home setting and primary care setting as a screening tool. FDA UDI
Model / Reference
HTD8813C FDA UDI
Description
Non Contact Infrared Body Thermometer designed to be used for intermittent measurement and monitoring of human bod temperature by consumers in the home setting and primary care setting as a screening tool. FDA UDI

Identifiers

Primary DI / UDI-DI
00050428313671 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intermittent electronic patient thermometer

CVS Pharmacy by Woonsocket Prescription Center, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a75058b7-9c35-4829-ac1c-0c1eead24a73 33 fields · synced May 30, 2026