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EUDAMED last updated this device on May 27, 2026
376038156CAFRAUPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Canule aspiratrice de Frazier boutonnée rigide Ø 2,0mm LU : 150mm is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Société Française de Fabrication d'Instruments de Chirurgie (SFFIC). Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
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 →03760381565396Basic 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 →376038156CAFRAUO33BRUDI 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 →(01)03760381565396
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
L030101SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLESterile
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 →No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market |
FR-MF-000019306No 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.376038156TMCRG6On the marketAnuscope de Bensaude adulte avec poignée intégrée dévissable Ø ext 22mm LU : 55mm376038156ANREBAPOn the marketAnuscope de Bensaude adulte pour manche éclaireur Ø ext 22mm LU : 55mm376038156ANREBAPOn the marketAnuscope de Bensaude moyen avec poignée intégrée dévissable Ø ext 20mm LU : 55mm376038156ANREBAPOn the marketAnuscope de Bensaude moyen avec poignée intégrée dévissable Ø ext 20mm LU : 70mm376038156ANREBAPOn the market