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PAWS Cruiser 16 - Fully automatic attachment
Classification
12 24 09 01 - Propulsion units for wheelchairs
The product series contains 2 products.
Product 1 of 2
PAWS Cruiser 16 - Fuld automatisk til og frakobling TETRA
HMI-no.
Article-no.
RPC16AAT00
Registration date
21-04-2021
Last updated
21-11-2023
Properties
User operated
Yes
Attendant operated
No
Measures
Battery capacity
11.7
Amperetimer
Weight
20.5
kg
Test information ![info](/en/img/i.svg)
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: Center for Testing and Certification, Warszawa, Poland. Test date: 31-08-2020
Test report for HMI-no. 129075
Test lab: Center for Testing and Certification, Warszawa, Poland. Test date: 31-08-2020
EU product safety regulation ![info](/en/img/i.svg)
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
PAWS Cruiser 16 - Fully automatic attachment
HMI-no.
Article-no.
RPC16AAS00
Registration date
21-04-2021
Last updated
21-11-2023
Properties
User operated
Yes
Attendant operated
No
Measures
Battery capacity
11.7
Amperetimer
Weight
20.5
kg
Test information ![info](/en/img/i.svg)
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: Center for Testing and Certification, Warszawa, Poland. Test date: 31-08-2020
Test report for HMI-no. 129074
Test lab: Center for Testing and Certification, Warszawa, Poland. Test date: 31-08-2020
EU product safety regulation ![info](/en/img/i.svg)
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device