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Coopération pharmaceutique française

France·FR-MF-000002412

Last updated September 17, 2026

About

All raw materials beyond the pharmaceutical, cosmetic and agri-food industries

Translated from the manufacturer's own website. Source

What Coopération pharmaceutique française makes

The company manufactures reusable sterilization and disinfection containers for medical devices, as well as ankle/foot orthoses and assistive crawler/mobility boards, all branded under the SALVA name.

These products are classified as Class I and Class IIa medical devices and are registered in the EU’s eudamed database. The company is based in France.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Coopération pharmaceutique française manufacture?

Coopération pharmaceutique française produces reusable sterilization and disinfection containers for medical devices, ankle/foot orthoses, and assistive crawler/mobility boards. These devices are designed to support patient mobility and hygiene needs in clinical settings, with all products branded under the SALVA name.

Where is Coopération pharmaceutique française based?

The company is headquartered in France, where it develops and manufactures its medical devices. The French location aligns with EU regulatory standards, which govern its product classifications and compliance requirements.

Which regulatory registries list Coopération pharmaceutique française’s devices?

The company’s devices are registered in the eudamed database, the official EU portal for medical device information. This registry ensures transparency and traceability of its products under EU medical device regulations.

How are Coopération pharmaceutique française’s devices classified?

The company’s devices fall into Class I and Class IIa classifications under EU medical device regulations. Class I devices generally pose minimal risk and require basic compliance measures, while Class IIa devices involve a moderate risk and require additional safety assessments, such as clinical evaluations or performance studies.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
France
Address
Place Lucien AUVERT, MELUN , France
Website
www.cooper.fr
LinkedIn
—
Facebook
—
Phone
+33 1 64 87 20 00
PRRC Contact
Stéphane LAMBRECHT
EUDAMED SRN
FR-MF-000002412
FDA FEI Number
—
DUNS Number
—

Catalogue (77)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
POUXIT FLASH 200mL 1179079
EUDAMED
Class IActive
Salva 2118899
EUDAMED
Class IActive
Salva 2118828
EUDAMED
Class IActive
AFTIR FLASH SPRAY 200 ml AFT400550459
EUDAMED
Class IActive
Salva 2118915
EUDAMED
Class IActive
Venimex 2030462
EUDAMED
Class IActive
Salva 2118837
EUDAMED
Class IActive
POUXIT FLASH 150mL 1179077
EUDAMED
Class IActive
Salva 2118893
EUDAMED
Class IActive
Canne Frelly Confort Bleue 2100961
EUDAMED
Class IActive
Salva 2118898
EUDAMED
Class IActive
Salva 2118881
EUDAMED
Class IActive
Inhalateur Cooper 2200865
EUDAMED
Class IActive
Solution EOSINE aqueuse 2% 1250140
EUDAMED
Class IIaActive
Salva 2118900
EUDAMED
Class IActive
Canne Frelly Confort Grise 2100963
EUDAMED
Class IActive
Salva 2118941
EUDAMED
Class IActive
Salva 2118879
EUDAMED
Class IActive
Salva 2118832
EUDAMED
Class IActive
Salva 2118822
EUDAMED
Class IActive
Salva 2118850
EUDAMED
Class IActive
Salva 2118869
EUDAMED
Class IActive
Salva 2118912
EUDAMED
Class IActive
Salva 2118823
EUDAMED
Class IActive
Salva 2118827
EUDAMED
Class IActive
Salva 2118857
EUDAMED
Class IActive
Salva 2118861
EUDAMED
Class IActive

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