All product information is provided by the supplier. The National Board of Social Services is not responsible for either contents, origin, flaws and deficiencies, or any kind of damage that may occur from the use of the information. The National Board of Social Services has no authority to endorse products and does not assess the quality of the products. Hide this message.

visolux DIGITAL XL FHD




Classification
22 03 18 07 - Handheld video magnifiers with an integrated monitor (CCTV)



The product series contains 2 products.

Product 1 of 2
Visolux Digital HD


HMI-no.
Article-no.
16521

Registration date
02-03-2021
Last updated
07-10-2022

Properties
HD Camera
Yes
Computer connection
Yes
TV connection
Yes
Battery-powered
Yes
Mains supply connection
Yes

Measures
Apparatus lenght
20
cm
info
The longest measure
Apparatus width
13.5
cm
Thickness
3
cm
Weight
0.460
kg
Monitor size
7
"
info
Diagonal measure
Magnification, min
2
Magnification, max
22

Test information
No information about tests according to standards info
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

CE-marking info
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
Medical Device Regulation (MDR) - 2017/745/EU


Product 2 of 2
Visolux DIGITAL XL FHD


HMI-no.
Article-no.
16551

Registration date
02-03-2021
Last updated
07-10-2022

Properties
HD Camera
Yes
Computer connection
Yes
TV connection
Yes
Battery-powered
Yes
Mains supply connection
Yes

Measures
Apparatus lenght
29
cm
info
The longest measure
Apparatus width
20
cm
Thickness
4
cm
Weight
1
kg
Monitor size
12
"
info
Diagonal measure
Magnification, min
2
Magnification, max
22

Test information
No information about tests according to standards info
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

CE-marking info
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
Medical Device Regulation (MDR) - 2017/745/EU