← 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 Micro Emerg Star Grip screw 1.9x4mm red self-tapping p/10 FDA UDI
Model / Reference
68.85.24A FDA UDI
Description
Ti Micro Emerg Star Grip screw 1.9x4mm red self-tapping p/10 FDA UDI

Identifiers

Catalog Number
68.85.24A FDA UDI
Primary DI / UDI-DI
04046826345839 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

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: 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

Manufacturer
Medicon eG. Chirurgiemechaniker-Genossenschaft

Sources (1)

  • FDA UDI b9b362fe-3475-4bf3-ab79-1b8dc5c794e2 35 fields · synced May 30, 2026