← Back to catalogue

MECRON Knee Straight L:500mm, OS:590mm, US:380mm

FDA UDI

Class I (US FDA UDI)

by Darco (Europe) GmbH

Identity

Trade Name
MECRON Knee Straight L:500mm, OS:590mm, US:380mm FDA UDI
Generic Name
Knee immobilizer FDA UDI
Device Name
XL Black 0° / 50 cm FDA UDI
Model / Reference
OS500404 FDA UDI
Description
XL Black 0° / 50 cm FDA UDI

Identifiers

Catalog Number
OS500404 FDA UDI
Primary DI / UDI-DI
00609271951174 FDA UDI
FDA Product Code
ITQ FDA UDI
GMDN Term
Knee immobilizer 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 immobilizer

A comprehensive knee immobilizer device used for temporary support and immobilization of the knee, offering a durable and adjustable option for various medical needs.

Similar devices

Also classified as Knee immobilizer.

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 df66076d-fa3d-4d81-b977-1ed6dcf8c95b 34 fields · synced Jul 22, 2026