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Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Skin treatment/dressing-supportive limb/finger bandage, reusable FDA UDI
Device Name
Walgreens Finger Sleeve w/Gel Insert 2s FDA UDI
Model / Reference
230820 FDA UDI
Description
Walgreens Finger Sleeve w/Gel Insert 2s FDA UDI

Identifiers

Primary DI / UDI-DI
00311917153445 FDA UDI
FDA Product Code
ILH FDA UDI
GMDN Term
Skin treatment/dressing-supportive limb/finger bandage, 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

No

FDA UDI

Single Use

No

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 treatment/dressing-supportive limb/finger bandage, reusable

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

Similar devices

Also classified as Skin treatment/dressing-supportive limb/finger bandage, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 39a67ab8-7f52-4109-a927-1c62bb60d960 34 fields · synced May 31, 2026