Information

The Class IIa medical device is subject to regular functional and safety inspections in accordance with applicable legislation.
A trained person performs this inspection at specified intervals, following a set procedure, to ensure the device’s safety and effectiveness.

For a medical device used by a healthcare provider, the first safety and technical inspection is prescribed by the manufacturer after 2 years from the date of commissioning.
Subsequent inspections are scheduled after 12 months.
After 10 years from commissioning, each subsequent inspection is required after 6 months.

Medical devices intended for individual use in home care are subject to their first safety inspection by the manufacturer 2 years after the date on which the medical device was introduced into service.
Subsequent inspections are scheduled after 24 months.
After 10 years of operation, a subsequent inspection is required every 12 months.
In the event of non-compliance with this recommendation, the manufacturer may not be held liable for any damages.

For medical devices equipped with a lithium battery (rechargeable battery), preventive safety inspections must be performed every 12 months from the date the device was put into operation.

The safety inspection is carried out by the manufacturer or an authorized organization.
Based on the results of the inspection, the service life of the medical device may be extended.
If the preventive safety inspection identifies that the medical device is not capable of safe operation, is not capable of fulfilling its intended purpose, or is irreparable, the service life of the medical device expires.

How to get a free extended warranty?
You only need a few minutes. Register your device for free using the form on this page,
fill in all required fields, carefully read and agree to the terms and conditions.
We will then send you a confirmation email to confirm that the guarantee has been obtained.

Production of the medical device is active as of 4 November 2020.

Software version
Current firmware: 1v014

Version of the instructions
You can request the current or older version of the manual from the manufacturer.

Current printed materials T4 (17 March 2026 REV E 26/03)
Instructions for Use – en
Bedienungsanleitung – de
Manual de uso – es
Manuel d‘utilisation – fr
Instrukcja obsługi – pl
Návod na použitie – sk
Návod k použití – cs
Istruzioni per l‘uso – it
Manual de instruções – pt
Navodila za uporabo – sl
Інструкція з експлуатації – uk
Hướng dẫn sử dụng – vi
Manual de utilizare – ro
Használati útmutató – hu
Руководство по эксплуатации – ru
Upute za uporabu – hr

Older printed materials T4
17 October 2023 REV D 23/10
31 March 2022 REV C 22/03
6 January 2021 REV B 21/01
22 October 2020 REV A 20/10

Important user information and instructions
Download valid product and system certificates for BIOMAG® products.
Older versions can be requested from the manufacturer.

Production of the medical device is active as of 4 November 2020.

Software version
Current firmware: Lu3DeV209

Version of the instructions
You can request the current or older version of the manual from the manufacturer.

Current printed materials T5 (17 March 2026 REV F 26/03)
Instructions for Use – en
Bedienungsanleitung – de
Instrukcja obsługi – pl
Használati útmutató – hu
Navodila za uporabo – sl
Návod na použitie – sk
Návod k použití – cs
Manual de uso – es
Istruzioni per l‘uso – it
Manual de utilizare – ro
Інструкція з експлуатації – uk
Hướng dẫn sử dụng – vi
Manuel d‘utilisation – fr
Manual de instruções – pt
Руководство по эксплуатации – ru
Upute za uporabu – hr

Older printed materials T5
17 October 2023 REV E 23/10
31 March 2022 REV D 22/03
17 February 2021 REV C 21/02
14 January 2021 REV B 21/01
22 October 2020 REV A 20/10

Important user information and instructions
Download valid product and system certificates for BIOMAG® products.
Older versions can be requested from the manufacturer.

Production of the veterinary technical device has been active since 15.04.2025.

Software version
Current firmware: 1v014

Version of the instructions
You can request the current or older version of the manual from the manufacturer.

Current printed materials TV2 (21 May 2025 REV A 25/05)
Instructions for Use – en
Bedienungsanleitung – de
Manual de uso – es
Manuel d’utilisation – fr
Instrukcja obsługi – pl
Návod na použitie – sk
Návod k použití – cs

Important user information and instructions
Download valid product and system certificates for BIOMAG® products.
Older versions can be requested from the manufacturer.

Production of the veterinary technical device has been active since 15.04.2025.

Software version
Current firmware: Lu3DeV209

Version of the instructions
You can request the current or older version of the manual from the manufacturer.

Current printed materials TV3 (21 May 2025 REV A 25/05)
Instructions for Use – en
Bedienungsanleitung – de
Manual de uso – es
Manuel d’utilisation – fr
Instrukcja obsługi – pl
Návod na použitie – sk
Návod k použití – cs

Important user information and instructions
Download valid product and system certificates for BIOMAG® products.
Older versions can be requested from the manufacturer.

Product range available in the Magnetotherapy Accessories section.

Maintain and disinfect leatherette products with Sani-Cloth® Active,
or another product with the same composition.
These are alcohol-free disinfectant wipes intended for disinfecting surfaces in all types
of healthcare facilities.
Instructions for use are provided on the product packaging.
In the home environment, it is recommended to clean as needed, but at least once a month.
Thinners and other chemical solvents must not be used to clean or maintain accessories.

Important user information and instructions
Certificates and declarations of conformity can be requested from the manufacturer.

BIOMAG® Lumina VET
Production of the veterinary technical device was discontinued on 14 October 2025.

Software version
Firmware: 1v231

Issued printed materials TV1
You can request a printed or electronic version of the instructions for use from the manufacturer.

Instructions for Use – en
15 April 2021 REV D 21/04
15 May 2018 REV Cb 18/05
20 April 2018 REV Ca 18/04
18 November 2014 REV A 14/11

Návod k použití – cs
12.04.2021 REV D 21/04
28.02.2018 REV Ca 18/02
21.03.2016 REV B 16/03
23.09.2013 REV A 13/09

Bedienungsanleitung – de
16.05.2018 REV Ca 18/05
16.07.2016 REV B 16/07
21.10.2013 REV A 13/10

Manual de uso – es
14/03/2018 REV Ca 18/03
22/03/2016 REV B 16/03
24/04/2014 REV A 14/04

Manuel d’utilisation – fr
15/04/2021 REV D 21/04
13/11/2013 REV A 13/11

Istruzioni per l’uso – it
30/03/2018 REV Ca 18/03
11/10/2015 REV B 15/10

Instrukcja obsługi – pl
15.04.2021 REV D 21/04
16.05.2018 REV Ca 18/05
10.03.2015 REV A 15/03

Manual de instruções – pt
16/03/2018 REV Ca 18/03

Руководство по эксплуатации – ru
15.04.2021 REV D 21/04

BIOMAG® LightFit Duo
Production of the medical device was discontinued on 31.01.2024

Software version
Firmware: 2.00

Issued printed materials T7
You can request a printed or electronic version of the instructions for use from the manufacturer.

Instructions for Use – en
31 March 2022 REV C 22/03
18 February 2021 REV B 21/02

Návod k použití – cs
31.03.2022 REV C 22/03
18.02.2021 REV B 21/02
22.01.2021 REV A 21/01

Manual de uso – es
31/03/2022 REV C 22/03
18/02/2021 REV B 21/02

Használati útmutató – hu
2022.03.31 REV C 22/03
2021.02.18 REV B 21/02

Istruzioni per l’uso – it
31/03/2022 REV C 22/03

Manual de instruções – pt
31/03/2022 REV C 22/03

BIOMAG® LightFit
Production of the medical device was discontinued on 11.03.2021.

Software version
Firmware: 1.12

Issued printed materials T3
You can request a printed or electronic version of the instructions for use from the manufacturer.

Instructions for Use – en
3 April 2020 REV F 20/04
11 September 2017 REV Ca 17/09
10 June 2015 REV A 15/06

Návod k použití – cs
22.10.2020 REV G 20/10
18.03.2020 REV F 20/03
20.12.2018 REV Ea 18/12
01.05.2018 REV Da 18/05
15.08.2017 REV Ca 17/08
30.09.2015 REV B 15/09
20.02.2015 REV A 15/02

Bedienungsanleitung – de
15.05.2019 REV Ea 19/05

Manual de uso – es
22/05/2018 REV Da 18/05
20/02/2015 REV A 15/02

Használati útmutató – hu
2018.12.07 REV Da 18/12
2017.08.21 REV Ca 17/08

Istruzioni per l’uso – it
11/05/2018 REV Da 18/05

Instrukcja obsługi – pl
17.05.2019 REV Ea 19/05

BIOMAG® Lumio
Production of the medical device was discontinued on 11.03.2021.

Software version
Firmware: 328V126

Issued printed materials T2
You can request a printed or electronic version of the instructions for use from the manufacturer.

Instructions for Use – en
3 April 2020 REV H 20/04
11 November 2016 REV D 16/11
1 June 2013 REV A 13/06

Návod k použití – cs
22.10.2020 REV I 20/10
30.10.2019 REV H 19/10
20.12.2018 REV Ga 18/12
29.03.2018 REV Fa 18/03
14.09.2017 REV Ea 17/09
30.06.2016 REV B 16/07
04.11.2013 REV A 13/11

Bedienungsanleitung – de
03.04.2018 REV Fa 18/04
11.11.2016 REV D 16/11
30.09.2015 REV C 15/09
01.06.2013 REV A 13/06

Manual de uso – es
01/06/2013 REV A 13/06

Manuel d’utilisation – fr
01/06/2013 REV A 13/06

Upute za uporabu – hr
04.11.2013 REV A 13/11

Használati útmutató – hu
2019.02.08 REV Ga 19/02
2018.01.08 REV Eb 18/01
2017.10.17 REV Ea 17/10
2013.06.01 REV A 13/06

Istruzioni per l’uso – it
16/10/2017 REV Ea 17/10
03/11/2013 REV A 13/11

Instrukcja obsługi – pl
30.11.2018 REV Fa 18/11
25.01.2017 REV C 17/01
18.07.2016 REV B 16/07
04.11.2013 REV A 13/11

Návod na použitie – sk
04.11.2013 REV A 13/11

Navodila za uporabo – sl
07.08.2020 REV H 20/08
28.02.2020 REV Ga 20/02

BIOMAG® Lumina
Production of the medical device was discontinued on 11.03.2021.

Software version
Firmware: 1v231

Issued printed materials T1
You can request a printed or electronic version of the instructions for use from the manufacturer.

Instructions for Use – en
3 April 2020 REV I 20/04
1 June 2018 REV Ga 18/06
7 September 2017 REV Fb 17/09
3 April 2017 REV Fa 17/04
1 December 2016 REV E 16/12
18 July 2016 REV D 16/07
8 March 2016 REV C 16/03
1 June 2015 REV B 15/06
1 June 2013 REV A 13/06

Návod k použití – cs
22.10.2020 REV J 20/10
18.03.2020 REV I 20/03
20.12.2018 REV Ha 18/12
30.05.2018 REV Ga 18/05
30.06.2017 REV Fb 17/06
31.03.2017 REV Fa 17/03
16.09.2016 REV D 16/09
11.02.2016 REV C 16/02
30.09.2015 REV B 15/11
01.06.2013 REV A 13/06

Bedienungsanleitung – de
03.04.2020 REV I 20/04
01.06.2018 REV Ga 18/06
07.09.2017 REV Fb 17/09
03.04.2017 REV Fa 17/04
01.12.2016 REV E 16/12
18.07.2016 REV D 16/07
01.06.2015 REV B 15/06
08.03.2016 REV A 16/03
01.06.2013 REV A 13/06

Manual de uso – es
31/05/2020 REV I 20/05
21/03/2019 REV Ha 19/03
19/10/2017 REV Fa 17/10
18/05/2016 REV B 16/05
01/06/2013 REV A 13/06

Manuel d’utilisation – fr
15/05/2020 REV I 20/05
08/10/2019 REV Ha 19/10
14/12/2018 REV Ga 18/12
10/01/2018 REV Fa 18/01
16/09/2016 REV D 16/09
25/11/2015 REV B 15/11
01/06/2013 REV A 13/06

Használati útmutató – hu
2020.04.10 REV I 20/04
2019.05.31 REV Ha 19/05
2017.04.26 REV Fa 17/04
2016.07.11 REV C 16/07
2015.09.15 REV B 15/09
2013.06.01 REV A 13/06

Istruzioni per l’uso – it
15/05/2020 REV I 20/05
08/10/2019 REV Ha 19/10
14/12/2018 REV Ga 18/12
10/01/2018 REV Fa 18/01
16/09/2016 REV D 16/09
25/11/2015 REV B 15/11
01/06/2013 REV A 13/06

Instrukcja obsługi – pl
10.04.2020 REV I 20/04
31.05.2019 REV Ha 19/05
26.04.2017 REV Fa 17/04
11.07.2016 REV C 16/07
15.09.2015 REV B 15/09
01.06.2013 REV A 13/06

Manual de instruções – pt
31/05/2020 REV I 20/05
21/03/2019 REV Ha 19/03
19/10/2017 REV Fa 17/10
18/05/2016 REV B 16/05
01/06/2013 REV A 13/06

Руководство по эксплуатации – ru
31.05.2020 REV I 20/05
18.10.2017 REV Fa 17/10
01.06.2013 REV A 13/06

Návod na použitie – sk
18.03.2020 REV I 20/03
20.12.2018 REV Ha 18/12
30.05.2018 REV Ga 18/05
30.06.2017 REV Fb 17/06
31.03.2017 REV Fa 17/03
16.09.2016 REV D 16/09
11.02.2016 REV C 16/02
30.09.2015 REV B 15/11
01.06.2013 REV A 13/06

Інструкція з експлуатації – uk
31.05.2020 REV I 20/05
18.10.2017 REV Fa 17/10
01.06.2013 REV A 13/06

Hướng dẫn sử dụng – vi
31/05/2020 REV I 20/05
26/04/2019 REV Ha 19/04
01/06/2013 REV A 13/06