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Copperfit

FDA UDI

Class I (US FDA UDI)

by Ideavillage Products Corp.

Identity

Trade Name
Copperfit FDA UDI
Generic Name
Orthotic insole, prefabricated, antimicrobial FDA UDI
Device Name
CopperFit Arch Relief Plus OS BLACK FDA UDI
Model / Reference
CFARSWOS FDA UDI
Description
CopperFit Arch Relief Plus OS BLACK FDA UDI

Identifiers

Primary DI / UDI-DI
00810179880484 FDA UDI
FDA Product Code
ITW FDA UDI
GMDN Term
Orthotic insole, prefabricated, antimicrobial 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

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthotic insole, prefabricated, antimicrobial

Copperfit by Ideavillage Products Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20c91d86-27b4-40d4-82d0-8dc1d74603f3 33 fields · synced Jun 8, 2026