← Back to catalogue

KERRAPED™ All Purpose Boot

FDA UDI

Class I (US FDA UDI)

by Darco (Europe) GmbH

Identity

Trade Name
KERRAPED™ All Purpose Boot FDA UDI
Generic Name
Orthotic shoe, non-customized FDA UDI
Device Name
M Black Round-toe FDA UDI
Model / Reference
KP2B FDA UDI
Description
M Black Round-toe FDA UDI

Identifiers

Catalog Number
KP2B FDA UDI
Primary DI / UDI-DI
00609271000261 FDA UDI
FDA Product Code
KNP FDA UDI
GMDN Term
Orthotic shoe, non-customized 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthotic shoe, non-customized

KERRAPED™ All Purpose Boot by Darco (Europe) GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic shoe, non-customized.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Darco (Europe) GmbH

Sources (1)

  • FDA UDI ad167d92-8edc-4011-ab0f-2e0d09a2eda9 34 fields · synced May 30, 2026