- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 16, 2023
3661489CHEVILLECIRMPDEASYMOVE SPATULE T3-T4 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by FOURNITURES HOSPITALIERES INDUSTRIE. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03661489716911271691(01)03661489716911
European Medical Device Nomenclature — the EU product classification assigned to this device.
L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER1 warning recorded — scroll inside the panel to see all entries.
FR-MF-000000819The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in France; available across 4 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | May 15, 2023 | Jan 1, 2050 |
| Germany | — | Still on market |
| Italy | — | Still on market |
| Poland | — | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
3661489CHEVILLECIRNMRDOn the marketEASYMOVE SPACER POUR GUIDE EP63661489CHEVILLECIRNMRDOn the marketEASYMOVE SPACER POUR GUIDE EP83661489CHEVILLECIRNMRDOn the marketEASYMOVE SPATULE T53661489CHEVILLECIRMPDOn the marketEASYMOVE SPATULE T6-T73661489CHEVILLECIRMPDOn the marketEASYMOVE SPOON CANNULATED SCREW3661489CHEVILLECIRMPDOn the marketCertificate health across this manufacturer's portfolio.
38944SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
40423AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
40315AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
40362AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
40417AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
40256AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →