Type Examination

Type Examination is a conformity assessment procedure in which a Notified Body evaluates a representative product sample (the "type") to verify compliance with applicable EU legislation. It is a key element of several CE marking modules and serves as a foundation for demonstrating product compliance when third-party involvement is required.

Role in EU Conformity Assessment

Type Examination is defined under Module B of the EU’s conformity assessment framework. It is typically used in conjunction with Modules C, F, or G, depending on the production and control requirements.

As part of the process, a Notified Body:

• Reviews the manufacturer’s technical documentation

• Assesses the design and construction of the product

• Conducts or oversees necessary testing

• Issues an EU Type Examination Certificate, which serves as formal proof that the type complies with the essential requirements of the applicable directive(s), such as the Radio Equipment Directive (RED) or the Low Voltage Directive (LVD).

Use Cases

Type Examination is commonly required for:

• Radio and telecommunications equipment

• Medical devices

• Machinery and pressure equipment

• Products involving high safety or interference risks

Related Services

Need EU type examination for a wireless device? Learn more about recognized procedures and coordination with Notified Bodies on our CE conformity assessment services and certification body network.