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.

Dokumentasjon

Datablad

Product Inspection Guide

Veiledning til produktinspeksjonsteknologi
Last ned de nye veiledningene om produktinspeksjon, som inneholder alt du behøver å vite om å skape et effektivt program for produktinspeksjon i produ...

Rapporter

Sikkerhet for legemidler – Sammenligning av standarder i EU og USA
Dette white paperet forklarer de juridiske rammeverkene som EU og USA har tatt til seg, og de endelige kravene for legemiddelbedrifter. Det sammenlign...
Forsegling på legemiddelpakninger
Dette white paperet forklarer betydningen av EU-direktiv 2011/62/EU og EN 16679 og hvilken påvirkning de vil ha på legemiddelpakninger. Det tar spesif...
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...
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.
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...

Saksstudier

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.
Rottendorf Pharma Advanced Technology
R-Pharm Germany GmbH has rounded out its service portfolio with the Case Aggregation Kit from METTLER TOLEDO PCE – in combination with a compatible ca...
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T2620 Serialization System

Tilbehør

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T2620 Serialization System

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