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Well At Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Well At Walgreens FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Moist Burn Pads, all one size, 2 in x 3 in (50 mm x 75 mm) FDA UDI
Model / Reference
157670 FDA UDI
Description
Moist Burn Pads, all one size, 2 in x 3 in (50 mm x 75 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00311917143835 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial 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-nonadherent dressing, absorbent, non-antimicrobial

Well At Walgreens by Walgreen Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 98549e2e-df5e-47ed-800e-418cc43fd896 34 fields · synced May 30, 2026