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Excellent Rampe System, SLIPSTOP
Classification
18 30 18 02 - Component parts for fixed ramps
Documents
User manualThe product series contains 4 products.
The product series also includes 3 discontinued products. Include discontinued products.
Product 1 of 4
Excellent SlipStop Flise
HMI-no.
47737
Article-no.
12830-farvekode
Registration date
12-02-2008
Last updated
22-08-2024
Test information
No information about tests according to standards 
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
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 4
Excellent SlipStop Rampe
HMI-no.
47738
Article-no.
12840-farvekode
Registration date
12-02-2008
Last updated
22-08-2024
Test information
No information about tests according to standards
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
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 3 of 4
Excellent SlipStop Rampe I
HMI-no.
47740
Article-no.
12850-farvekode
Registration date
12-02-2008
Last updated
22-08-2024
Test information
No information about tests according to standards
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
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 4 of 4
Excellent SlipStop Rampe II
HMI-no.
47743
Article-no.
12860-farvekode
Registration date
12-02-2008
Last updated
22-08-2024
Test information
No information about tests according to standards
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
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