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Free Webinar: Direct Marking for UDI Compliance

By aisltd, Monday, 27th June 2016 | 0 comments
Filed under: Industry News.

The next deadline in the FDA's Unique Device Identification (UDI) regulation will hit September 24, 2016 – and it's not just about your medical device packaging anymore! Register here.

The FDA requires that any medical device intended for multiple uses and subject to reprocessing must bear a UDI directly marked on the device itself. In this webinar, arm yourself with knowledge about current UDI marking guidance and methodologies, with answers to questions such as: 

- What does it mean to "permanently mark" a device? 
- Which medical devices require direct marks? 
- What are the deadlines for permanent UDI marking? 
- Does the FDA require a specific marking method? 
- What can be done to ensure mark quality and compliance? 

Join Microscan Training Coordinator and Certified GS1 Standards Professional, Barbie LaBine, as she presents current FDA UDI guidelines for marking devices with permanent marks, marking methods, and verification solutions.

Should you wish to speak to one of our highly experienced Engineers about the implications of the UDI regulation on your packaging, please contact us today.

Dublin

Automatic Identification Systems Ltd

Cork

Automatic Identification Systems Ltd
Unit 35 Eastgate Drive,
Little Island, Cork,  
T45 C925, Ireland

Phone: +353 (0)21 235540
Fax: +353 (0)1 6205735
Email: info@aisltd.ie

Barcelona

AIS Vision Systems S.L
Pol. Ind. Can Roqueta,
Avda. Can Bordoll, 119 Sabadell,
Barcelona 08202, Spain

Phone: +34 931 003 035
Fax: +34 931 003 038
www.aisvision.com

Beugen

AIS-Scanology B.V. 
Laan de Wijze 20,
5835 DS Beugen
The Netherlands

Phone: +31 (0)485-561616
Fax: +31 (0)485-561610
www.scanology.nl

 

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