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Knee Separator

FDA UDI

Class I (US FDA UDI)

by Walgreen Health Solutions, LLC

Identity

Trade Name
KNEE SEPARATOR FDA UDI
Generic Name
Leg/knee cushion FDA UDI
Device Name
KNEE SEPARATOR, Leg/Knee Cushion (One Size) FDA UDI
Model / Reference
831727004664 FDA UDI
Description
KNEE SEPARATOR, Leg/Knee Cushion (One Size) FDA UDI

Identifiers

Catalog Number
831727004664 FDA UDI
Primary DI / UDI-DI
G0648317270046640 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Leg/knee cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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: Leg/knee cushion

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

Similar devices

Also classified as Leg/knee cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2a67688f-d82f-4e47-8a8e-cc797416c391 35 fields · synced May 30, 2026