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CVS Health

FDA UDI

Class II (US FDA UDI)

by Woonsocket Prescription Center, Incorporated

Identity

Trade Name
CVS Health FDA UDI
Generic Name
Electric pad localized-body heating system FDA UDI
Device Name
Electrical Heated Therapy Patch - ePatch Refill Kit FDA UDI
Model / Reference
MEP300R FDA UDI
Description
Electrical Heated Therapy Patch - ePatch Refill Kit FDA UDI

Identifiers

Catalog Number
395100 FDA UDI
Primary DI / UDI-DI
04719873873012 FDA UDI
FDA Product Code
IRT FDA UDI
GMDN Term
Electric pad localized-body heating system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5740 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0444431e-c929-47a6-9ba8-ed3313f3072e 35 fields · synced May 31, 2026