UDI Marking

UDI requirements in the US

Put into effect in the US in September 2013, the UDI system gradually became mandatory a year later in September 2014. Adoption of the UDI system began on the following dates in other countries where production of US-bound medical devices exists.

Refer to: GS1 Healthcare Japan conference “Operational guide to direct marking on to medical devices”

Need for direct marking

Steel medical instruments, such as endoscopes, are generally compact and precise. Repeated use after washing and sterilizing is common, so paper and film display labels are problematic due to limited space for affixing and lack of long-term durability.

There are also unacceptable risks in terms of medical practices, such as a label coming off during surgery and becoming residual foreign particles within a patient’s body.

这些问题导致了日益增长的需要use a system that incorporates a direct marking method.

Advantages

Managing medical equipment through direct marking offers the following advantages:

• Quality control by monitoring how frequently tools are used
• Optimized part replacement and ordering
• Improved efficiency and standardization of instrument sets
• In-process instrument tracking (location management)
• Excess stock control
• Loss and theft analysis

What kind of marking is necessary?

The following GS1 code is used for direct marking on medical instruments.

• GS1-128
• GS1 Data Matrix (if surface area for GS1-128 cannot be ensured)

以下信息必须提供使用as a display item.

• 01: GTIN (product code) / 10: Lot no. / 17: Expiration date
• 21: Serial no. / 11: Manufacturing date

These two-digit numbers are called AI (application identifiers). If the numbers are meant to be expressed as visible characters, they must be surrounded by parentheses ( ).

GTIN: 4569951110016
Serial number: 42345A-2
(01)04569951110016 (21)42345A-2

The display size of direct marking on medical instruments and other healthcare products as specified in the GS1 standard is as noted in the following table.

Excerpt from GS1 system symbol specification table 7 in the GS1 General Specifications

Advantages of cold marking

Laser marks on medical devices typically fall into the following categories:

Oxidation
This method involves using the heat of the laser to color the surface of a target black.

Engraving
This method involves increasing the laser irradiation density to remove the surface of a target.

Cold marking
This method involves coloring the surface of a target black without removing the oxidized film.

Many medical components have a chromium exterior, which turns into chromium carbide when heat is applied (thus reducing its corrosion-resistance). Conventional near-IR lasers use heat to create black contrast, which risks causing corrosion over time. UV lasers - thanks to photolytic processing - can mark parts without damaging the surface material.

Ability to mark extremely small codes

Controlling the laser beam size makes it possible to create minute markings as small as 0.5 mm × 0.5 mm (0.02" x 0.02") even when marking a 26-digit (18 × 18 cells) GTIN or serial number in a GS1 data matrix.