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Rite Aid Pharmacy

FDA UDI

Class I (US FDA UDI)

by Rite Aid Corporation

Identity

Trade Name
RITE AID PHARMACY FDA UDI
Generic Name
Corn/callus dressing, single-use FDA UDI
Device Name
Hydrocolloid Gel Blister Cushions, all one size, 1.65 IN x 2.67 IN (42 mm x 68 mm) FDA UDI
Model / Reference
011822037341 FDA UDI
Description
Hydrocolloid Gel Blister Cushions, all one size, 1.65 IN x 2.67 IN (42 mm x 68 mm) FDA UDI

Identifiers

Catalog Number
00371678 FDA UDI
Primary DI / UDI-DI
00011822037341 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Corn/callus dressing, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
Not 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

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

Rite Aid Pharmacy by Rite Aid Corporation — Class I — 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 51d0cf0d-f1a0-4d35-bf72-146baf1e510d 35 fields · synced May 30, 2026