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Empulse F55
Classification
12 24 48 01 - Pivot drive wheels units
Documents
The product series contains 2 products.
Product 1 of 2
Empulse F55 14
HMI-no.
126348
Registration date
08-10-2020
Last updated
24-04-2025
Measures
Battery capacity
8.1
Amperetimer
Weight
11
kg
Test information 
Though the product is testet, it might not have passed all requirements in the standard. Besides, some products are only tested according to parts of the standard. Read the test report for detailed information. See also other standards that could be relevant for this product type.
EN 12182:1999: Technical aids for disabled persons - General requirements and test methods.
Test lab: TÜV SÜD Product Service GmbH. Test date: 27-01-2020
Test report for HMI-no. 126348
Test lab: TÜV SÜD Product Service GmbH. Test date: 27-01-2020
EU product safety regulation 
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device
Product 2 of 2
Empulse F55 8.5
HMI-no.
126347
Registration date
08-10-2020
Last updated
24-04-2025
Measures
Battery capacity
8.1
Amperetimer
Weight
11
kg
Test information 
Though the product is testet, it might not have passed all requirements in the standard. Besides, some products are only tested according to parts of the standard. Read the test report for detailed information. See also other standards that could be relevant for this product type.
EN 12182:1999: Technical aids for disabled persons - General requirements and test methods.
Test lab: TÜV SÜD Product Service GmbH. Test date: 27-01-2020
Test report for HMI-no. 126347
EN 12184:2014: Electrically powered wheelchairs, scooters and their chargers - Requirements and test methods.
Test lab: TÜV SÜD Product Service GmbH. Test date: 27-01-2025
Test report for HMI-no. 126347
Test lab: TÜV SÜD Product Service GmbH. Test date: 27-01-2020
EN 12184:2014: Electrically powered wheelchairs, scooters and their chargers - Requirements and test methods.
Test lab: TÜV SÜD Product Service GmbH. Test date: 27-01-2025
EU product safety regulation 
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device