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Medicon Epiplating System

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon Epiplating System FDA UDI
Generic Name
Cranial bur, reusable FDA UDI
Device Name
counterbore dental shaft FDA UDI
Model / Reference
68.80.50 FDA UDI
Description
counterbore dental shaft FDA UDI

Identifiers

Catalog Number
68.80.50 FDA UDI
Primary DI / UDI-DI
04046826409708 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Cranial bur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cranial bur, reusable

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

Similar devices

Also classified as Cranial bur, 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 46f0e929-268a-401a-82a9-70bd6d723ec5 34 fields · synced May 30, 2026