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Capteur Protect

France FR-MF-000037387 Last updated 21 Oct 2026

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Devices
158
Registries
EUDAMED
FDA recalls
0

Catalogue158

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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.

Translated from the manufacturer's own website. Source

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.

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 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.

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

Information

Country
France
Address
15, rue Jean Charcot, ROMANS SUR ISERE, France
PRRC contact
Denise GALZERANO
EUDAMED SRN
FR-MF-000037387