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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
Burn kit, non-medicated FDA UDI
Device Name
3-Step Kit for Minor Burns, 6 pieces: gauze pads, hydrogel burn pads, rolled gauze. FDA UDI
Model / Reference
310381 FDA UDI
Description
3-Step Kit for Minor Burns, 6 pieces: gauze pads, hydrogel burn pads, rolled gauze. FDA UDI

Identifiers

Primary DI / UDI-DI
00050428616802 FDA UDI
FDA Product Code
OJJ FDA UDI
GMDN Term
Burn kit, non-medicated 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

No

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

Yes

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: Burn kit, non-medicated

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

Similar devices

Also classified as Burn kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 45ef143b-a78c-44e8-a8e6-55cf85de3995 33 fields · synced May 30, 2026