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Rite Aid

FDA UDI

Class I (US FDA UDI)

by Rite Aid Corporation

Identity

Trade Name
Rite Aid FDA UDI
Generic Name
Skin-cover adhesive strip, non-antimicrobial FDA UDI
Device Name
Waterproof, Flexible Foam, Sterile Adhesive Pad, all one size, Dressing- 3.5 IN x 4.5 IN (88 mm x 114 mm), Pad Size- 2 IN x 3 IN (50 mm x 76 mm) FDA UDI
Model / Reference
011822089142 FDA UDI
Description
Waterproof, Flexible Foam, Sterile Adhesive Pad, all one size, Dressing- 3.5 IN x 4.5 IN (88 mm x 114 mm), Pad Size- 2 IN x 3 IN (50 mm x 76 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00011822089142 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Skin-cover adhesive strip, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-cover adhesive strip, non-antimicrobial

Rite Aid by Rite Aid Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-cover adhesive strip, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI abb616c1-feee-40a6-95ee-3f7451ff3c46 34 fields · synced May 30, 2026