ENSURE THE REGULATORY QUALITY
OF EACH OF
OUR PRODUCTS
Medistock guarantees the conformity of the medical devices it markets.
The entire manufacturing chain, from design to finished product, is subject to strict controls.
We work with high-performance industrial partners and have established rigorous quality control and traceability procedures, to ensure that our products comply with European and international standards.
A TEAM
dEDICATED TO qualitY.
Several years ago, MEDISTOCK set up a Quality and Regulatory Affairs department.
This specialized team is committed to the control, quality managment and regulatory compliance of medical devices.
Thanks to its expertise, it proactively adapts to regulatory and normative developments in the medical sector.
Medistock IS
ISO 13485 CERTIFIED
MEDISTOCK is certified by a notified body wich guarantees that the quality management system mets the requirements of the medical standard EN ISO 13485 : 2016.
NOTICES
rEGULATORY
The products presented are Class I, Is and IIa, Medical Devices, and carry the CE mark, in accordance with Directive 93/42/CE and/or Regulation (UE) 2017/745.
These devices, manufactured by MEDISTOCK, are intented for healthcare professionals.
Indications for Class IIa DM are specified on each item.
CE conformity assessment has been carried out by MTIC (CE0068) for class Is et IIa.
Products bearing the LPPR code are reimbursed by health insurance organizations.
Please consult the label or leaflet of each device before use.
Some of the products shown are made by other manufacturers. These products are class I, Is and IIa and are CE marked by their manufacturers respectively in accordance with Regulation (UE) 2017/745 and/or directive 93/42/CEE.