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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Canule aspiratrice Courbe rigide… — Class I MDR

MD Atlas
Société Française de Fabrication d'Instruments de Chirurgie (SFFIC)

EUDAMED last updated this device on May 26, 2026

Canule aspiratrice Courbe rigide Ø 4,0mm LU : 105mm

376038156CACGX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Société Française de Fabrication d'Instruments de Chirurgie (SFFIC)
UDI-DI code: 03760381564405
Reference / catalog number: O135

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Manufacturer information

Organization name: Société Française de Fabrication d'Instruments de Chirurgie (SFFIC)
SRN: FR-MF-000019306
Manufacturer status: Active

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Certificates

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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: Canule aspiratrice Courbe rigide Ø 4,0mm LU : 105mm
UDI-DI code: 03760381564405
Basic UDI-DI: 376038156CACGX
Reference / catalog number: O135
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

L030101SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, REUSABLE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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