Certificates

Certificates of the MTR+ Vertriebs GmbH

MTR+ Vertriebs GmbH takes great value, that all customers or business partners can be sure, to buy their products from a serious company. For this reason we run a quality management which is checked regularly by an independent institution (notified body).
Expression of the successful quality control of the company is the certificate of approval, shown below (DIN EN ISO 13485:2016).

The quality management of course also extends on the products. All our equipment is quality controlled and fulfills the regulations of the german law (MPG) as well as the underlying EC guideline 93/42/EEC for medicine products. The equipment therefore bears the CE sign with the following four-digit number for the examining institute. (CE 0123 means, that our device are comply with the EC-requirements).

G10 MDR-certificate
of 2023-12-06
PDF: G10-certificate

Certifiate ISO 13485:2016
of 2023-05-30
PDF: ISO 13485

 

Declaration of conformity of our devices

 

F.A04.07(DOC)-001-01 – Declaration of Conformity (EU)-Dolobravo

F.A04.07(DOC)-002-01 – Declaration of Conformity (EU)-Rehabravo

F.A04.07(DOC)-003-01 – Declaration of Conformity (EU)-Biobravo

F.A04.07(DOC)-004-01 – Declaration of Conformity (EU)-Myobravo

F.A04.07(DOC)-087-01 – Declaration of Conformity (EU)-SineBravo

F.A04.07(DOC)-089-01 – Declaration of Conformity (EU)-DuoBravo U

F.A04.07(DOC)-090-01 – Declaration of Conformity (EU)-DuoBravo N

F.A04.07(DOC)-112-01 – Declaration of Conformity (EU)-PeroBravo

F.A04.07(DOC)-188-01 – Declaration of Conformity (EU)-IontoBravo

F.A04.07(DOC)-200-02 – Declaration of Conformity (EU)-Dolito

F.A04.07(DOC)-201-01 – Declaration of Conformity (EU)-Rehalito

F.A04.07(DOC)-202-01 – Declaration of Conformity (EU)-Biolito

F.A04.07(DOC)-205-01 – Declaration of Conformity (EU)-Myolito

 

 
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