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DARCO® Toe Cap

FDA UDI

Class I (US FDA UDI)

by Darco (Europe) GmbH

Identity

Trade Name
DARCO® Toe Cap FDA UDI
Generic Name
Foot friction/impact protector FDA UDI
Device Name
MXL Black for Relief Dual® FDA UDI
Model / Reference
TCDBM4 FDA UDI
Description
MXL Black for Relief Dual® FDA UDI

Identifiers

Catalog Number
TCDBM4 FDA UDI
Primary DI / UDI-DI
00609271247437 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Foot friction/impact protector 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot friction/impact protector

DARCO® Toe Cap by Darco (Europe) GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Foot friction/impact protector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Darco (Europe) GmbH

Sources (1)

  • FDA UDI eb48d875-e9b0-4050-811b-008e2a0e50f4 34 fields · synced May 29, 2026