Skip to content

+41766405728 Asti (IT) / Zug (CH) / Shanghai (CN) / Stevenage (UK) info@advanxa.eu

EU Market Access – Auth. Rep. and Consulting services

EU Auth. Rep. service
CE Mark
MDR / EUDAMED
- MDR Support request
- UDI/EUDAMED SUPPORT
Swiss Aut Rep
UKCA
- UK Responsible Person support
Smart Certificate Validator
Reach out
Search for:

Reach out

Your name

Your email

Company name

Subject

Device Type

MDR Medical DeviceMachinery DirectiveLow Voltage DirectiveEMC DirectivePPEOther

Your message (optional)

Our Services

EU Auth. Rep. service
CE Mark
MDR / EUDAMED
- MDR Support request
- UDI/EUDAMED SUPPORT
Swiss Aut Rep
UKCA
- UK Responsible Person support
Smart Certificate Validator
Reach out

International Medical Device Registration Guidances

USA Regulatory Framework Medical Device registration
Taiwan Regulatory Framework Medical Device registration
South Korea Regulatory Framework Medical Device registration
South Africa Regulatory Framework Medical Device registration
Singapore Regulatory Framework Medical Device registration
Saudi Arabia Regulatory Framework Medical Device registration
Russia Regulatory Framework Medical Device registration
Peru Regulatory Framework Medical Device registration
Malaysia Regulatory Framework Medical Device registration
Japan Regulatory Framework Medical Device registration
Canada Regulatory Framework Medical Device registration
China Regulatory Framework Medical Device registration
Costa Rica Regulatory Framework Medical Device registration
Egypt Regulatory Framework Medical Device registration
Hong Kong Regulatory Framework Medical Device registration
India Regulatory Framework Medical Device registration
Reach out

Auth. Rep. Support

CE Mark
e-IFU Software solution

MDR / EUDAMED

Reach out