T2620| for Marking & Verification of Pharmaceutical Products

T2620 Serialization System

Safety through Serialization Compact, fully integrated system for marking and verification of pharmaceutical Track & Trace products

GMP Compliant Design
The T2620 features easily-accessible parts for cleaning and maintenance, in compliance with Good Manufacturing Processes (GMP).

Compatible with Existing ERP Systems
The T2620 runs on the complete PCE software suite, allowing seamless integration into pre-existing ERP, MES or cloud environments.

Compact Product Design
Space is normally at a premium in production sites, so the T2620 was designed with a small footprint in order to minimize spatial requirements.

T2620 Serialization System

T2620 Specification Table

Product Width (mm) 25-150
Product Height (mm) 10 - 100
Field of View (height x width in mm) 95 x 70
Max Linear Line Speed (m/min)80
RejectorAir blast, high-performance air blast, pusher

Click the image below to view the diagram.

T2620 Features and Benefits

System Flexibility
Suitable for a diverse range of packaging sizes and types with quick product changeovers. Adjustable to line speeds of up to 400 parts per minute (ppm).
Centralized Track & Trace Management
Management of all Track & Trace systems, from manual stations through to complete solutions in high-speed packaging lines including aggregation and database entry using PCE Line Manager (PLM).
Datamatrix Grading
In-line validation printed datamatrix code quality according to ISO 15415 to ensure advanced line performance
Global Service and Support
A global service network supports cross-border contracts and ensures timely support and the availability and quick delivery of spare parts to reduce downtime and keep processes running smoothly.

Documentation

Datasheets

Product Inspection Guide

Guide to Product Inspection Technology
Download the new product inspection guides detailing everything you need to know about building an effective product inspection programme in manufactu...

White Papers

Understanding Regulations in Medical Device Labeling
This white paper looks at the aggregation process which defines the track and trace data relationship between the parent and child.
Tamper-Evident Pharmaceutical Packaging
This white paper explains the implications of the EU directive 2011/62/EU and EN 16679 and how this will affect pharmaceutical packaging. It specifica...
Serialization - Are You Ready?
The global threat of counterfeit medicines is growing. Quickly learn how to reliably track and trace medicinal products by integrating serialization s...
Security of Pharmaceuticals - Comparing US and EU Standards
This white paper describes the legal frameworks adopted by the European Union and the United States and the resulting requirements for pharmaceutical...
Food Safety Standards and Legislation White Paper
This white paper looks at the Communicating Reliable Information and Standards for Agriculture and Logistics (CRISTAL); a communications framework for...

Case Studies

State-of-the-Art Track & Trace Solution
The XMV datamatrix station from METTLER TOLEDO PCE supports August Faller in providing sustainable marking and verification of cardboard boxes, carton...
Medac Serialises Products for Safety
In this case study pharmaceutical company Medac successfully uses a combination of checkweigher and marking system to achieve serialisation requiremen...
Artesan Pharma Implement Serialization Early
An early adopter of serialization technology, Artesan Pharma could offer serialization services to customers far in advance of regulatory deadlines.

Accessories

Multimedia

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T2620 Serialization System
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