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Brochure downloads

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Catalogues and Brochures Directions for use Data sheets Declaration of conformity ISO / EC Certificates Campaigns

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Preparation

R-PILOT

RECIPROC® blue instruments

RECIPROC® instruments

Mtwo®

FlexMaster®

RECIPROC® direct

VDW 6 : 1 SIRONA Contra-Angle

VDW.CONNECT® App for DE, EN, FR, IT, ES, BR

VDW.CONNECT® App for BG, SK, HR, HU, DA, SV, KO

VDW.CONNECT® App for CS, PL, RO, TR, EL

VDW.CONNECT® App for SL, NO, NL, LV, LT, FI, ET

VDW.CONNECT Drive® for DE, EN, FR, IT, ES

VDW.CONNECT Drive® for BG, SK, HR, HU, DA, SV, KO

VDW.CONNECT Drive® for CS, PL, RO, TR, BR, EL

VDW.CONNECT Drive® for SL, NO, NL, LV, LT, FI, ET

VDW.CONNECT Drive® Accessories iPad stand

VDW.CONNECT Locate® for EN

VDW.CONNECT Locate® for ES

VDW.CONNECT Locate® for FR

VDW.CONNECT Locate® for IT

VDW.CONNECT Locate® for KO

VDW.CONNECT Locate® for TR

VDW.GOLD® RECIPROC®  for DE, EN, FR, IT, ES

VDW.GOLD® RECIPROC® for CZ, PL, RO, TR, PT, EL

VDW.GOLD® RECIPROC® for RU, ZH, KO, SR, HU, SV, DA, HR

VDW.GOLD® RECIPROC® Upgrade for DE, EN, FR, ES, RU

VDW.GOLD® RECIPROC® Upgrade for CZ, PL, RO, PT

VDW.GOLD® RECIPROC® Upgrade for ZH, SR, HU, HR, DA

VDW.GOLD® RECIPROC® Erratum EN

VDW.GOLD®

VDW.SILVER® RECIPROC® for DE, EN, FR, IT, ES

VDW.SILVER® RECIPROC® for CZ, PL, RO, TR, EL, PT, HR

VDW.SILVER® RECIPROC® for RU, ZH, KO, SR, SV, DA, HU

VDW.SILVER® RECIPROC® Upgrade

VDW.SILVER® for DE, EN, FR, IT, ES

VDW.SILVER® for ZH, CZ, DA, EL, PL, PT, RU, SV

RAYPEX® 6 for DE, EN, FR, IT, ES

RAYPEX® 6 other languages

RAYPEX® 5

VDW.ROTATE™ for DE, EN, FR, IT, ES, PT, NL, SV, DA, CS, PL

VDW.ROTATE™ for RO, TR, EL, UK, RU, JA, KO, SR, HU, PTB, ID, AR

SDS - Safety data sheets

“The medical device manufacturer VDW GmbH is certified according to EN ISO 13485:2016. The company’s marketable products are fully subject to the regulatory provisions of Council Directive 93/42/EEC of 14 June 1993 on medical devices and bear the corresponding CE marking.

Within the framework of the corresponding requirements, all materials used by the company are also secured and checked in accordance with Regulation (EC) no 1907/2006. In accordance with the product design, the finished products are also validated for safety and efficacy and the corresponding labelling is made available to the user/customer, in line with labelling regulations. Based on the applicable requirement, the manufacturer is not subject to any further provisions according to (EC) no 1907/2006 (2) safety data sheets for finished products.”

ISO / EC Certificates

VDW is certified manufacturer of medical devices according to 93/42/EEC.

VDW EG Certificate G1 (valid until 2024.05.26)

VDW EG Certificate G2S Sterile Root Canal Instruments (valid until 2024.05.26)

VDW ISO13485:2016 (valid until 2022.05.26)

MDSAP Certificate (valid until 2022.04.17)

Old for Gold

Exchange your old endo device for a new one VDW.GOLD®RECIPROC® with an additional payment of only 1.725,– €* We exchange your old endo device with date of purchase before 31.12.2015

Your responsible VDW sales representative or your internal sales team are happy to help:

by phone: + 49 ( 0) 89 / 6 27 34 - 444
by fax: + 49 ( 0) 89 / 6 27 34 - 274
by e-mail: endo(at)vdw-dental.com

Please keep the serial number of your old device ready when ordering. Delivery and calculation takes place via the dental trade. Processing and instruction are carried out by the responsible VDW sales rep.

Download your flyer here.

Your VDW Team

*The prices are exclusive of VAT.

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