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TurnAssist®

FDA UDI

Class I (US FDA UDI)

by Walgreen Health Solutions, LLC

Identity

Trade Name
TurnAssist® FDA UDI
Generic Name
Patient transfer/turning sheet, single-use FDA UDI
Device Name
TurnAssist® Premium Repositioning Glide Sheet, Patient Transfer/Turning Sheet. Size Standard FDA UDI
Model / Reference
831727001472 FDA UDI
Description
TurnAssist® Premium Repositioning Glide Sheet, Patient Transfer/Turning Sheet. Size Standard FDA UDI

Identifiers

Catalog Number
831727001472 FDA UDI
Primary DI / UDI-DI
G0648317270014720 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Patient transfer/turning sheet, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 34.5 Inch FDA UDI
Length — 58 Inch FDA UDI

Category: Patient transfer/turning sheet, single-use

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

Similar devices

Also classified as Patient transfer/turning sheet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bef97791-440b-42de-ac82-8812b93b0ddd 36 fields · synced May 30, 2026