0035 - NOTIFIED BODY (UNDER DIRECTIVE 93/42/EEC Medical devices) 
Name and address of the notified bodie
Responsible for the following products
Responsable for the following procedures/modules
Annexes/articles of the directives

TÜV BERLIN-BRANDENBURG e.V.

TÜV -CERT-ZERTIFIZIERUNGSSTELLE für Medizinprodukte

Magirusstrasse , 5

12103 Berlin
GERMANY

T : 00 49 30 7562 1365
F : 00 49 30 7562 1364
URL :
Email :
bienert@de.tuv.com

  • dental equipment,
  • disinfection and sterilization equipment,
  • protheses and rehabilitation devices,
  • Patient storage and transport equipment,
  • medical supply units,

Active medical devices :

  • vital-parameter monitoring and plotting devices,
  • equipment for infusions,
  • anaesthesia devices, repirators and oxygen therapy equipment,
  • surgical equipment and ancillary surgical equipment,
  • imaging equipment :
    • with ionizing radiation,
    • with non-ionizing radiation,
  • stimulation devices
  •  radiotherapy equipment with non-ioninzing radiation
  • ophtalmological devices

 

Type-examination
EC verification

Annex III
Annex IV


site - http://www.hosmat.fr - dernière mise à jour / last update : 6 novembre 1999