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CVS Health

FDA UDI

Class I (US FDA UDI)

by Woonsocket Prescription Center, Incorporated

Identity

Trade Name
CVS Health FDA UDI
Generic Name
Wound hydrogel dressing, non-sterile FDA UDI
Device Name
Hydrogel Burn Pads, all one size, 1.96 IN x 2.95 IN (49 mm x 74 mm) FDA UDI
Model / Reference
832833 FDA UDI
Description
Hydrogel Burn Pads, all one size, 1.96 IN x 2.95 IN (49 mm x 74 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00050428277447 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Wound hydrogel dressing, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wound hydrogel dressing, non-sterile

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

Similar devices

Also classified as Wound hydrogel dressing, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f2a52aa1-1d1f-4728-b4a4-222338fb9af9 34 fields · synced Jun 8, 2026