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Flowtron Hydroven 12
Classification
04 06 09 03 - Air-filled attachments and pulsating compression systems, arm
The product series contains 4 products.
Product 1 of 4
Flowtron Hydroven 12 insertion textile, arm 68 cm
HMI-no.
41897
Article-no.
316AI68
Registration date
11-11-2005
Last updated
20-02-2024
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
Flowtron Hydroven 12 insertion textile, arm 78 cm
HMI-no.
41896
Article-no.
316AI78
Registration date
11-11-2005
Last updated
20-02-2024
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
Flowtron Hydroven 12, arm 68 cm
HMI-no.
42096
Article-no.
316A68
Registration date
13-12-2005
Last updated
20-02-2024
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
Flowtron Hydroven 12, arm 78 cm
HMI-no.
41895
Article-no.
316A78
Registration date
11-11-2005
Last updated
20-02-2024
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