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Foot Compression Wrap Medium

FDA UDI

Class I (US FDA UDI)

by Sun-Scientific Inc.

Identity

Trade Name
Foot Compression Wrap Medium FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
Aero-Wrap™ Foot Compression Wrap is designed to provide therapeutic compression therapy, in the inpatient and outpatient setting, in the treatment of edema and lymphedema of the foot or as part of a wound treatment protocol. FDA UDI
Model / Reference
MW5260 FDA UDI
Description
Aero-Wrap™ Foot Compression Wrap is designed to provide therapeutic compression therapy, in the inpatient and outpatient setting, in the treatment of edema and lymphedema of the foot or as part of a wound treatment protocol. FDA UDI

Identifiers

Catalog Number
FCW-200 FDA UDI
Primary DI / UDI-DI
00850051939237 FDA UDI
FDA Product Code
MHW FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

Yes

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: Compression/pressure sock/stocking, reusable

Foot Compression Wrap Medium by Sun-Scientific Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sun-Scientific Inc.

Sources (1)

  • FDA UDI d263dbc2-27fd-4e8e-b6ab-e23ecbff805d 36 fields · synced May 30, 2026