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Michel Gillmann of Xerafy provides a converter’s guide to moving from a promising RFID component to a repeatable finished label.
September 4, 2026
By: Greg Hrinya
By Michel Gillmann, Co-Founder and Chief Marketing Officer, Xerafy
The first test looked successful. A thin on-metal RFID label produced strong reads on an enterprise laptop. But when several laptops were stored closely together, that same performance exposed a different problem: a reader could also capture adjacent devices.
This was a real source-tagging program supported by Xerafy. The label had to be applied upstream so every laptop entered service with its RFID identity already in place, then remain manageable through a four-year lifecycle. Success therefore depended not only on RF performance, but also on printability, serialization, roll format, packaging, quality control, and reprints.
The lesson was simple: a good inlay is only the starting point. The finished label must work on the product, through production, and in the operating process.
The five decisions below draw on Xerafy’s work with converters and end users across enterprise IT and medical sterilization projects.
The first decision is not “How far can it read?” but “Where must it read, and where must it stop?” Define the label position, reader geometry, item density, and intended read points before selecting the inlay.
Metal housings, coatings, curves, metallized films, and nearby liquids can all change performance. On metal, the label may need an on-metal construction or spacer. Near liquids, placement or a barrier layer can matter. In the laptop program, the approved specification covered both reliable reads at the chosen point and control of unwanted reads from neighboring devices.
Terms such as “high temperature,” “autoclave resistant” or “gamma compatible” describe a challenge, not a test. The relevant question is what the complete label must survive: temperature, duration, cycles, pressure, radiation dose, chemicals, washing, abrasion, or handling between processes.
Xerafy received a similar starting brief across several medical-device projects: provide a UHF label that remained functional after about 50 kGy of gamma sterilization. That brief quickly expanded to include the tagged surface, adhesive and facestock, printing and encoding, roll format, and data requirements. Final acceptance depended on testing the converted label after irradiation (not only the inlay) and confirming RF performance, memory integrity, adhesion, and print legibility.
The practical lesson: translate every environmental claim into an exposure sequence and a clear result after exposure.
When an inlay becomes a label, every added layer can change the result. Facestock affects print quality, flexibility, and resistance. Adhesive must suit the actual surface and lifecycle. Spacers and barrier layers can become part of RF performance near metal or liquids. Lamination can add protection while changing thickness, flexibility, and antenna behavior.
More material is not automatically better. The objective is the simplest repeatable stack that meets the application. Low profile and chip placement also matter when the customer needs a large uninterrupted print face or when exposed edges could snag in use.
Printing should then be checked as a system: facestock, ribbon or ink, heat, speed, and expected durability.
A label that reads correctly but cannot run reliably through converting, printing, or encoding is not production-ready. Before samples are made, agree on four things: the required supply format – dry inlay, wet inlay or finished label; the web and roll specification, including width, pitch, and winding direction; the printer and encoder; and the serialization and reprint rules.
These decisions belong in the product specification from the start. A repeatable roll and data format also makes source tagging possible, because the label can be applied by a manufacturer, converter, or service bureau before the finished product reaches the end user.
Samples alone do not constitute a qualification plan. A pilot should establish what passing looks like before anyone scales production.
At minimum, it should prove that labels can be converted, printed, and encoded consistently; remain attached and readable after the required exposure; perform at the intended read points without excessive cross-reads; and remain consistent from roll to roll. Testing should use representative products, placements, readers, and operating density.
The output should be a controlled specification covering the approved construction and placement, production settings, acceptance criteria, and route for replacements or reprints.
Not every specialty project needs a custom antenna or long development program. The faster route is usually to start with the closest proven platform, change only what the application and production process require, and validate the finished result.
This also provides a commercial filter. If the customer cannot yet define the surface, exposure, production format or acceptance test, the project is not ready for scale pricing. Once those answers are available, the converter can move more confidently from sample to repeatable production.
That same discipline applies when RFID is added at source, embedded in a product, incorporated through in-mold labeling or used to support Digital Product Passports.
Xerafy helps converters enter these demanding applications without developing every RFID construction from scratch. Start with a field-proven specialty RFID platforms for metal, liquids, sterilization, or other industrial and healthcare conditions, then adapt only the materials, format and validation the project requires. Bring us the application challenge: we can help select the starting platform, define the construction and build a focused sample and validation plan.
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