Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name: WALGREENS FDA UDI
Generic Name: Tubular support bandage, non-latex, reusable FDA UDI
Device Name: WALG Copper Ankle Sleeve - M/L FDA UDI
Model / Reference: 973078 FDA UDI
Description: WALG Copper Ankle Sleeve - M/L FDA UDI

Identifiers

Primary DI / UDI-DI: 00049022942554 FDA UDI
FDA Product Code: IQI FDA UDI
GMDN Term: Tubular support bandage, non-latex, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3475 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Tubular support bandage, non-latex, reusable

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

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

Tubifast® — Mölnlycke Health Care AB · Class I
MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class I
Tubifast® — Mölnlycke Health Care AB · Class I
Tubifast® — Mölnlycke Health Care AB · Class I
ViveCare — VIVE HEALTH LLC · Class I
Juzo Suspension Sleeve — JULIUS ZORN, INC. · Class I
MediChoice — OWENS & MINOR DISTRIBUTION, INC. · Class I
Tubifast® — Mölnlycke Health Care AB · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Walgreen Co.

Sources (1)

FDA UDI a6861dc3-d2b5-4659-96af-69cef5cf2d6d 34 fields · synced Jun 8, 2026