Regulatory / Quality Assurance
Manufacturers of medical devices based outside the EU must designate
an Authorized Representative (EC-REP) established within the EU in order to meet
the CE requirements for placing medical devices on the EU market.
European Authorized Representative
Manufacturers of medical devices based outside the EU must designate an Authorized Representative (EC-REP) established within the EU in order to meet the CE requirements for placing medical devices on the EU market.
Authorized representative: |
Regen Lab France S.A.S |
Address: |
2 Avenue de Laponie, 91940 Les Ulis, France |
Contact person / e-mail: |
Office manager: Béatrice Montel, France@regenlab.com |
Phone: |
+33 1 42 00 22 90 |
MANUFACTURER
Legal Manufacturer |
REGEN LAB SA |
Address |
En Budron B2 |
Extension (storage area) |
En Budron C5 |
Phone |
+41 (0) 21 864 01 11 |
Fax |
+41 (0) 21 864 01 10 |
Contact Regenlab
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located in
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- Paris (France)
- Dubai (U.A.E.)
- Beijing (China)
- and Istanbul (Turkey)