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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
(10mm) CastWedge Cast Adjuster. Designed for cast realignment and swelling relief. Use with plaster or fiberglass cast. FDA UDI
Model / Reference
20831727009106 FDA UDI
Description
(10mm) CastWedge Cast Adjuster. Designed for cast realignment and swelling relief. Use with plaster or fiberglass cast. FDA UDI

Identifiers

Catalog Number
20831727009106 FDA UDI
Primary DI / UDI-DI
G064208317270091061 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 — 10 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

Sources (1)

  • FDA UDI 52e9dbe9-bc4e-406d-9b2b-e225aa37359c 36 fields · synced Jun 8, 2026