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Medicon

FDA UDI

Class I (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
General/plastic surgery bur FDA UDI
Device Name
burr fig 8 Ø 12mm FDA UDI
Model / Reference
76.50.18 FDA UDI
Description
burr fig 8 Ø 12mm FDA UDI

Identifiers

Catalog Number
76.50.18 FDA UDI
Primary DI / UDI-DI
04046826151744 FDA UDI
FDA Product Code
HXY FDA UDI
GMDN Term
General/plastic surgery bur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: General/plastic surgery bur

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

Similar devices

Also classified as General/plastic surgery bur.

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 6c14b2b7-2f67-44e8-8de2-e7ebf26ade6d 35 fields · synced Jun 6, 2026