UV Adhesive EU UFI Application Processing Guide
Date：2026-03-24 09:52:59 Classification
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UV Adhesive EU UFI Application Processing Guide
1、 Basic concepts of UFI
UFI (Unique Formula Identifier) is a key identification code in the European Union Centre for Toxicity of Chemicals Mixtures (PCN) system. UV glue, as a chemical mixture product, must complete UFI registration when sold in the EU market. This identifier is used to enable emergency centers to quickly identify product ingredients and take appropriate medical treatment measures in the event of a poisoning accident.
2、 Scope of application
UV glue for UFI application must meet the following conditions:
|Condition | Description
|Sales Market | Sales within the European Union and the European Economic Area (EEA)
|Product type | Chemical mixture (UV glue belongs to this category)
|Supply mode | Both B2B and B2C supply require processing
|Regulatory trigger point | The mixture contains ingredients that pose a health or physical hazard
3、 Handling process
1. Preparation stage
Collect complete formula information for UV glue
Confirm the concentration range and CLP classification of all ingredients
Prepare SDS (Safety Data Sheet) for the product
2. Formula submission
Login to ECHA (European Chemicals Agency) PCN submission portal
Choose the appropriate submission format (IUCLID or toxicology center specific format)
Fill in the mixture formula information, including:
CAS/EC numbers for each component
concentration range
Hazard classification
Physical and chemical properties
3. UFI generation
The system automatically generates a unique UFI code based on the recipe
Format: UFI: XXXX-XXXX-XXXXX-XXXX
Suggest using the UFI verification tool provided by ECHA for validation
4. Label update
Label the UFI code on the product label
Update Section 1.1 (Product Identifier) of SDS file
Ensure that both consumers and professionals can see UFI information
4、 Key precautions
|Number | Precautions | Detailed Explanation
|1 | Formula accuracy | The submitted formula must be completely consistent with the actual production formula, and any changes must be reapplied for
|2 | Concentration Range | Normal fluctuations between production batches should be considered, and the concentration range should be set reasonably
|3 | Hazard Classification | Accurate determination of CLP hazard classification is required, which affects the mandatory requirements of UFI
|4 | Submission Language | The official language version of the country where the product is sold must be provided
|5 | Official fees | ECHA itself does not charge fees, but service fees may be incurred through third-party platforms
5、 Time and Validity Period
Effective Date: Mandatory Enforcement from January 1, 2021
Review cycle: ECHA typically completes preliminary validation within a few days
Validity period: UFI is bound to a specific formula, and formula changes require reapplication
6、 Consequences of Violation
Failure to label UFI as required when selling UV glue in the EU market may result in:
Administrative penalties imposed by regulatory agencies of member states
The product is required to be withdrawn from the market
Legal litigation and economic compensation risks faced
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