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Total Comfort Knee Support Sleeve

FDA UDI

Class I (US FDA UDI)

by Home Aide Diagnostics, Inc.

Identity

Trade Name
Total Comfort Knee Support Sleeve FDA UDI
Generic Name
Tubular support bandage, non-latex, reusable FDA UDI
Device Name
Total Comfort Knee Support Sleeve Available in MD-XL FDA UDI
Model / Reference
4524 FDA UDI
Description
Total Comfort Knee Support Sleeve Available in MD-XL FDA UDI

Identifiers

Primary DI / UDI-DI
00850027494531 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Tubular support bandage, non-latex, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

Category: Tubular support bandage, non-latex, reusable

Total Comfort Knee Support Sleeve by Home Aide Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI be2b3a11-5fdb-482a-ba04-23fe4d31a887 34 fields · synced May 30, 2026