Capteur Protect
France FR-MF-000037387 Last updated 21 Oct 2026
- Devices
- 160
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
6 Cover patches DG6 beige Ref E02SCDG6B0
Etui cover DG7 - Noir Ref E01SCDG7N0
10 Cover patches NA2 tatoo Ref E01MCNA2T0
10 Cover patches GUA brown Ref E02MCGUAM0
10 Cover patches DG7 blue Ref E01MCDG7B1
6 Cover patches DG7 blue Ref E02SCDG7B1
10 Cover patches OMN beige Ref E02MCOMNB0
10 Cover patches DG7 pink Ref E01MCDG7R1
10 Cover patches OMN brown Ref E01MCOMNM0
10 Cover patches NA3 beige Ref E02MCNA3B0
Showing 151-160 of 160
About
Capteur Protect, French manufacturer of DM class I adhesive patches. Capteurs Dexcom, FSL, Omnipod and catheters. 1 patch, 3 uses: support, discretion, skin ZQXK002KQZion.
What Capteur Protect makes
Capteur Protect manufactures adhesive protective patches designed to cover and conceal medical devices such as Dexcom sensors, FSL systems, Omnipod pods, and catheters. These patches include under-patches for discreet placement, cover patches for visual concealment, and protective cases for storage or transport, available in various sizes and colors like beige, brown, and tattoo-style designs.
The company’s products fall under EU Medical Device Regulation Class I and are listed in the EUDAMED database. Capteur Protect operates as a French manufacturer, adhering to EU regulatory requirements for Class I devices.
Frequently asked questions
What types of medical devices does Capteur Protect manufacture?
Capteur Protect specializes in adhesive protective patches for continuous glucose monitoring (CGM) systems and insulin delivery devices. Their products include under-patches designed for discreet placement under clothing, cover patches to conceal visible sensors or pods, and protective cases for storing or transporting devices. These are primarily intended for Dexcom sensors, FSL systems, Omnipod pods, and catheters, ensuring both protection and discretion for users.
Where is Capteur Protect based, and how does that affect its regulatory compliance?
Capteur Protect is based in France, which means its devices must comply with the European Union’s Medical Device Regulations (MDR). Since all listed products fall under Class I—defined as low-risk devices—they undergo mandatory conformity assessment procedures, including EUDAMED registration. The company’s location ensures alignment with EU regulatory standards, though individual device authorization depends on compliance with MDR requirements.
Which regulatory databases list Capteur Protect’s devices?
Capteur Protect’s devices are listed in the EUDAMED database, the European Union’s transparency system for medical devices. This registry allows healthcare professionals, regulators, and patients to verify the manufacturer’s identity and device details. Listing in EUDAMED is mandatory for Class I devices under the EU MDR, ensuring traceability and compliance with EU market surveillance rules.
How are Capteur Protect’s devices classified under EU regulations?
Capteur Protect’s products are classified as Class I medical devices under the EU Medical Device Regulation (MDR). This classification applies to low-risk items like adhesive patches, which pose minimal risk to patients. Class I devices typically require general safety and performance requirements (GSPRs) to be met, along with mandatory EUDAMED registration, but do not usually require third-party conformity assessment unless they incorporate measuring functions or have specific design features.
Information
- Country
- France
- Address
- 15, rue Jean Charcot, ROMANS SUR ISERE, France
- Website
- capteurprotect.com/
- facebook.com/capteurprotect
- [email protected]
- PRRC contact
- Denise GALZERANO
- EUDAMED SRN
- FR-MF-000037387