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Medicon

FDA UDI

Class II (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
Orthopaedic fixation plate bending insert, reusable FDA UDI
Device Name
protecting screw cross slot p/10 f 2.4 locking system FDA UDI
Model / Reference
68.98.90 FDA UDI
Description
protecting screw cross slot p/10 f 2.4 locking system FDA UDI

Identifiers

Catalog Number
68.98.90 FDA UDI
Primary DI / UDI-DI
04046826405854 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Orthopaedic fixation plate bending insert, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 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

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate bending insert, reusable

Medicon by Medicon eG. Chirurgiemechaniker-Genossenschaft — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate bending insert, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medicon eG. Chirurgiemechaniker-Genossenschaft

Sources (1)

  • FDA UDI 68d7376e-1ced-4afc-8d02-f91db1de1464 35 fields · synced Jun 8, 2026