← Back to catalogue

Medicon

FDA UDI

Class II (US FDA UDI)

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Identity

Trade Name
Medicon FDA UDI
Generic Name
Craniofacial bone screw, non-bioabsorbable, non-sterile FDA UDI
Device Name
Ti Mini cross slot screw p/10 2x15 grey self-tapp fine thr. FDA UDI
Model / Reference
68.94.75A FDA UDI
Description
Ti Mini cross slot screw p/10 2x15 grey self-tapp fine thr. FDA UDI

Identifiers

Catalog Number
68.94.75A FDA UDI
Primary DI / UDI-DI
04046826485009 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Craniofacial bone screw, non-bioabsorbable, non-sterile 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

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

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 Unsafe FDA UDI

Category: Craniofacial bone screw, non-bioabsorbable, non-sterile

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

Similar devices

Also classified as Craniofacial bone screw, non-bioabsorbable, non-sterile.

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

Sources (1)

  • FDA UDI 857d2cbd-5a31-46a3-821a-a2bd9bff2af7 35 fields · synced May 30, 2026