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Hyperlight Therapy

Floor stand for Bioptron Pro 1

 

PAG-991-FS

BIOPTRON Pro1 is equipped also with a floor stand, which offers the maximum operation and handling support. The floor stand is delivered with flat feet, but a set of wheels is included as well.
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Retail price € 292.00
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RRP PRICE (€)  ≥
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Discount Level
≥ 10
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≥ 100
DL2 -10%
≥ 1000
DL3 -15%
≥ 2000
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≥ 3000
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≥ 5000
DL6 -30%
≥ 10000
DL7 -35%
≥ 20000
DL8 -40%
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RRP PRICE(€) ≥
+
Number of Members
ZepterClub
Discount Level
10

-
DL1 -5%
100

-
DL2 -10%
300

1
DL3 -15%
500

2
DL4 -20%
500

3
DL5 -25%
500

4
DL6 -30%
8000

20
DL7 -35%
15000

30
DL8 -40%
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Retail price € 292.00
Zepter Clubprice € 277.40
Quantity
Discount -5% € 14.60
Total price € 277.40
Delivery up to 21 days
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Overview

BIOPTRON Pro1 is equipped also with a floor stand, which offers the maximum operation and handling support. The floor stand is delivered with flat feet, but a set of wheels is included as well.

Presentation

The filter diameter of the BIOPTRON Pro1 (approx. 11 cm) allows the treatment of bigger areas of the body and it is suitable for the use at home, in hospitals and different therapeutic centres. 
The floor stand guarantees highest comfort in any application, being a comfortable support while handling.
 

Tech Data

Item code
PAG-991-FS
Product name
Floor stand for Bioptron Pro 1
Gross weight [KG]
6.45
Net weight [KG]
6.2
Application
Accessory to be used with Bioptron Pro 1
Producer
BIOPTRON AG - Sihleggstrasse 23, CH-8832 Wollerau - Switzerland
Made in
Switzerland
Color
White
Certifications/Declaration
* Declaration of Conformity with the medical Directive 93/42 / EEC issued by the producer. *Confirmation of application a medical device in the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products * CE conformity for electrical equipment. * Certificate for Quality Assurance (EN ISO 13485) * Certificate for the Quality Assurance System (Directive 93/42 / EEC) issued by the FDA * DEKRA Certificate for quality control EN ISO 13485:2012 + AC:2012 * DEKRA Certificate for medical devices complying with Annex II, Section 3 of Directive 93/42 / EEC - (Notified Body ID 0124) * Declaration of conformity from DEKRA (European notified body) for all products issued in 2013 (07.21.2013)

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