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CastWedge™

FDA UDI

Class I (US FDA UDI)

by Walgreen Health Solutions, LLC

Identity

Trade Name
CastWedge™ FDA UDI
Generic Name
Cast spreader, single-use FDA UDI
Device Name
(20 mm) CastWedge™ Cast Adjuster. Designed for cast realignment and swelling relief. Use with plaster or fiberglass cast. FDA UDI
Model / Reference
20831727009205 FDA UDI
Description
(20 mm) CastWedge™ Cast Adjuster. Designed for cast realignment and swelling relief. Use with plaster or fiberglass cast. FDA UDI

Identifiers

Catalog Number
20831727009205 FDA UDI
Primary DI / UDI-DI
G064208317270092051 FDA UDI
FDA Product Code
LGF FDA UDI
GMDN Term
Cast spreader, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5940 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Over-the-Counter

No

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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 20 Millimeter FDA UDI

Category: Cast spreader, single-use

CastWedge™ by Walgreen Health Solutions, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cast spreader, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Health Solutions, LLC

Sources (1)

  • FDA UDI 70f6656d-c098-4cda-9813-f5482a3ba666 36 fields · synced May 30, 2026