← Back to catalogue

3-teilige Universal Funktions-Knieschiene 20deg

FDA UDI

Class I (US FDA UDI)

by Darco (Europe) GmbH

Identity

Trade Name
3-teilige Universal Funktions-Knieschiene 20deg FDA UDI
Generic Name
Knee support orthosis FDA UDI
Device Name
50 cm Black FDA UDI
Model / Reference
OH30050 FDA UDI
Description
50 cm Black FDA UDI

Identifiers

Catalog Number
OH30050 FDA UDI
Primary DI / UDI-DI
00609271951457 FDA UDI
FDA Product Code
ITQ FDA UDI
GMDN Term
Knee support orthosis 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Knee support orthosis

3-teilige Universal Funktions-Knieschiene 20deg by Darco (Europe) GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee support orthosis.

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 e4625107-ec51-4d78-b777-720a15436522 34 fields · synced Jun 1, 2026