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FR-MF-000016213NICRALLIUM TA6VELI Poudre 20-63 microns is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by BERNARD CERVOS SOCIETE. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jun 15, 2022
376035797TAEPHQPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03760357972661
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in France; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Jun 15, 2022 | Jun 15, 2042 |
| Belgium | Jun 15, 2022 | Jun 15, 2042 |
| Germany | Jun 15, 2022 | Jun 15, 2042 |
| Spain | Jun 15, 2022 | Jun 15, 2042 |
| Italy | Jun 15, 2022 | Jun 15, 2042 |
| Netherlands | Jun 15, 2022 | Jun 15, 2042 |
| Poland | Jun 15, 2022 | Jun 15, 2042 |
| Portugal | Jun 15, 2022 | Jun 15, 2042 |
| Romania | Jun 15, 2022 | Jun 15, 2042 |
| Slovakia | Jun 15, 2022 | Jun 15, 2042 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03760357972661Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
376035797TAEPHQ0150TAEP2063UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q010601DENTAL ALLOYS376035797TAEPHQOn the marketNICRALLIUM TA6VELI Poudre 15-45 microns376035797TAEPHQOn the marketNICRALLIUM TA6VELI Poudre 20-53 microns376035797TAEPHQOn the marketNICRALLIUM TA6VELI Poudre 20-75 microns376035797TAEPHQOn the marketNICRALLIUM TA6VELI Poudre 45-106 microns376035797TAEPHQOn the marketPEEK P20 Disque Ø98,5x10mm376035797P20DC2On the marketNo certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.