Quality Management System

US FDA Good Manufacturing Practice (GMP)

Vidacare is registered with the Federal Drug Administration: FDA # 3004526033.

• Vidacare’s Establishment Registration and Device Listing
• ISO 13485:2003 Quality System Certification (PDF)
• Vidacare is certified to MDD and Canadian CMDCAS regulatory requirements via British Standards Institute (BSI).

Authorized Representative

Vidacare uses Emergo Europe as its Authorized Representative in Europe:

Emergo Europe
Molenstrast 15
2513BH, The Hague
The Netherlands
Telephone: +31.70.345.8570