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CopperUnder sock Small/Medium

FDA UDI

Class II (US FDA UDI)

by Sun-Scientific Inc.

Identity

Trade Name
CopperUnder sock Small/Medium FDA UDI
Generic Name
Compression/pressure sock/stocking, reusable FDA UDI
Device Name
A sock made with 40% MODAACRYLIC infused with copper polyester small/medium FDA UDI
Model / Reference
AW7025-00 FDA UDI
Description
A sock made with 40% MODAACRYLIC infused with copper polyester small/medium FDA UDI

Identifiers

Catalog Number
CS150 FDA UDI
Primary DI / UDI-DI
00850051939527 FDA UDI
FDA Product Code
LLK FDA UDI
GMDN Term
Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5780 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

CopperUnder sock Small/Medium by Sun-Scientific Inc. — Class II — 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 844f048c-6402-4f27-bb25-2b945dd7cf59 36 fields · synced Jun 1, 2026