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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
WALGREENS ANTI EMBOLISM STOCKNG KNEE HIGH SZ MED WHTE FDA UDI
Model / Reference
439488 FDA UDI
Description
WALGREENS ANTI EMBOLISM STOCKNG KNEE HIGH SZ MED WHTE FDA UDI

Identifiers

Primary DI / UDI-DI
00311917014050 FDA UDI
510(k) Number
K123820 FDA UDI
FDA Product Code
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5780 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Compression/pressure sock/stocking, reusable

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

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 635d430d-9734-4d78-a071-c7f5db538b4f 35 fields · synced May 31, 2026