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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
Sternal fixation device FDA UDI
Device Name
depht gauge f fixation FDA UDI
Model / Reference
54.81.05 FDA UDI
Description
depht gauge f fixation FDA UDI

Identifiers

Catalog Number
54.81.05 FDA UDI
Primary DI / UDI-DI
04046826495770 FDA UDI
FDA Product Code
HRS FDA UDI
GMDN Term
Sternal fixation device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

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
MRI Safety
MR Conditional FDA UDI

Category: Sternal fixation device

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

Similar devices

Also classified as Sternal fixation device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7851adf9-3796-4fee-9d75-2b29751fef77 35 fields · synced May 31, 2026