Epoxy AB Glue EU UFI Registration Process
Date：2026-05-18 09:54:10 Classification
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EU UFI Registration Process for Epoxy Resin AB Glue
I. Preliminary Preparation Stage
1. Confirm UFI Registration Requirements
Scope of Application: Epoxy resin AB glue containing hazardous components under the CLP Regulation (such as skin sensitization, corrosion, etc.) must complete UFI registration before being placed on the EU market.
Regulatory Basis: EU CLP Regulation (Regulation EC No 1272/2008) and Poison Center Notification (PCN) requirements.
Special Characteristics of AB Glue: Attention must be paid to the independent classification of components A and B before mixing, and the classification changes of the final product after mixing.
2. Product Information Collection
| Materials Prepared | Specific Content
| Formulation Information | Complete composition and concentration of each component A/B
| Hazard Classification | Physical, health, and environmental hazard classification based on CLP
| Application Information | Instructions for industrial/professional/consumer use
| Packaging Specifications | Packaging type and size range
| Routes of Exposure | Exposure routes such as inhalation, skin contact, and eye contact
II. Core Registration Process
3. Hazard Assessment and Classification
Perform CLP hazard assessments separately for Component A and Component B.
Perform a comprehensive hazard assessment for the final product after mixing.
Identify all applicable hazard categories and declaration label elements.
4. ECHA Portal Submission
1. Account Registration: Create a company account on the ECHA portal website.
2. Mixture Declaration: Select Submit.
3. Information Completion:
Mixture Identification Information (Name, Formulation)
Hazard Classification Details
Toxicological Information
Exposure Scenarios and First Aid Measures
4. UFI Generation: The system automatically generates a unique UFI number based on the formulation information.
Format Example: UFI: XXXX-XXXX-XXXX-XXXX
5. Labeling Requirements
Clearly label the UFI number on the product label.
Other CLP labeling requirements must also be met (hazard pictograms, signal words, precautionary statements, etc.).
Consumer products must additionally include first aid medical information.
III. Precautions and Subsequent Maintenance
6. Key Special Considerations
Formulation Changes: Any change in ingredients affecting hazard classification requires a resubmission of the UFI.
Multi-purpose Products: Different uses of the same product must be submitted separately or clearly distinguished.
Supply Chain Transmission: UFI information must be transmitted to downstream users.
7. Official Fees and Timeline
Fees: Submission through the ECHA portal is currently free (subject to change).
Timeline: Approximately one week if all materials are complete.
Validity: Registration information requires continuous updating and maintenance.
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