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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

1316INFL-2.5150 — Class IIa MDR by EUROMI

MD Atlas
EUROMI

EUDAMED last updated this device on May 20, 2026

1316INFL-2.5150

3701416250000CAN3G

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EUROMI
UDI-DI code: 03701416200745
Reference / catalog number: 1316INFL-2.5150

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Manufacturer information

Organization name: EUROMI
SRN: BE-MF-000014212
Manufacturer status: Active

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

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Belgium; available across 1 country total.

Country	On market since	Until
BelgiumPrimary placement	Mar 27, 2009	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03701416200745
Basic UDI-DI: 3701416250000CAN3G
Reference / catalog number: 1316INFL-2.5150
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: CANULE D'INFILTRATION MANUELLE MODELE LUER INOX DIAMETRE 2,5 LONGUEUR 150
Additional information URL: https://www.euromi.com/fr/doc-professionnelle/
Clinical sizes: 150 MU50
2.5 MU50

EMDN nomenclature code(s)

L250301LIPOSUCTION CANNULAS, 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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