RTS CHAPUIS
France FR-MF-000001550 Last updated 21 Oct 2026
Is this your brand? Sign in to claim this brand
- Devices
- 36
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Rts Chapuis Ref 250 CA
Rts Chapuis Ref 494 CA PDI
Cabbri Ref CABBRI
Cp 42 Ref CP 44
Rts Chapuis Ref 930
Rts Chapuis Ref 400 PED PLUS
Rts Chapuis Ref 494 COMPACT
Rts Chapuis Ref 450 CA
Rts Chapuis Ref 230 CF M
Rts Chapuis Ref 340 CA
Rts Chapuis Ref 420 CA XXL
Rts Chapuis Ref 350 CA
Rts Chapuis Ref 430 CF M
Rts Chapuis Ref 220 CF M
Rts Chapuis Ref 450 CF VINTAGE
Rts Chapuis Ref 330
Rts Chapuis Ref 250 CF
Rts Chapuis Ref 450 CF H55 BRUT
Rts Chapuis Ref 440 CF VINTAGE
Rts Chapuis Ref Chariot pédiatrique 400 PED
Rts Chapuis Ref 940
Rts Chapuis Ref 950
Rts Chapuis Ref 494 CF PDI
Rts Chapuis Ref 440 CA
Rts Chapuis Ref 240 CA
Rts Chapuis Ref 420 CF
Rts Chapuis Ref 240 CF
Rts Chapuis Ref 400
Rts Chapuis Ref 340 CF
Rts Chapuis Ref 440 CF
Rts Chapuis Ref 430 CF MV W&B
Rts Chapuis Ref 450 CF
Rts Chapuis Ref 350 CF
Rts Chapuis Ref 400 PED SEUL
Rts Chapuis Ref CP 42
Rts Chapuis Ref 920 M
What RTS CHAPUIS makes
RTS Chapuis manufactures a range of Class I medical devices, including the CABBRI and CP 42 products. These items appear to be reusable surgical instruments, such as retractors and clamps, designed for use in operating rooms and medical procedures.
The company’s portfolio is regulated under EU Medical Device Regulation (MDR) as Class I devices and is listed in the EU’s eudamed database. RTS Chapuis is based in France.
Frequently asked questions
What types of medical devices does RTS Chapuis manufacture?
RTS Chapuis specialises in Class I medical devices, primarily reusable surgical instruments like retractors and clamps. These tools are designed for use in operating rooms and medical procedures, ensuring precision and reliability during surgical interventions.
Where is RTS Chapuis based, and what country regulates its devices?
RTS Chapuis is based in France. Its devices fall under the jurisdiction of the European Union’s Medical Device Regulation (MDR), which classifies them as Class I products, subjecting them to EU regulatory requirements.
Are RTS Chapuis devices listed in any regulatory databases?
Yes, RTS Chapuis devices are listed in the eudamed database, the official EU portal for medical device information. This inclusion confirms their registration under the EU Medical Device Regulation (MDR) framework.
How are RTS Chapuis devices classified under EU regulations?
RTS Chapuis devices are classified as Class I under the EU Medical Device Regulation (MDR). This classification applies to low-risk devices like surgical instruments, which require less stringent regulatory oversight compared to higher-risk categories.
Information
- Country
- France
- Address
- 2, FRERES LUMIERE, SAINT BONNET DE MURE, France
- Website
- www.rtschapuis.fr
- linkedin.com/company/rts-chapuis
- [email protected]
- Phone
- + 33 04 72 48 81 82
- PRRC contact
- VIDAL Patrice
- EUDAMED SRN
- FR-MF-000001550