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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

KIT 007 — Class IIa MDR by MED EUROPE EUROPEAN…

MD Atlas
MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL

EUDAMED last updated this device on Apr 23, 2026

KIT 007

803360952CANNULEG9

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
UDI-DI code: 08033609528493
Reference / catalog number: KIT 007

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View device family (Basic UDI)

Manufacturer information

Organization name: MED EUROPE EUROPEAN MEDICAL SUPPLIES SRL
SRN: IT-MF-000026962
Manufacturer status: Active

Related devices

PD-DS-2015803360952CANNULEG9On the market SIM 1-150cc803360952ACCESSORI-DRENNKOn the market MED ST-32 PVCB-08033609525126On the market TRACHEA SUCTION SET803360952ACCESSORI-DRENNKOn the market PAC 3.4 B-08033609524877On the market

Certificates

Certificate health across this manufacturer's portfolio.

0425-MDR-030102-00Issued
Quality management systemNotified body: 0425Expiry: Oct 17, 2029

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW011
Il dispositivo non deve essere utilizzato a contatto con trapani o strumenti che potrebbero danneggiare l'integrità del dispositivo stesso; in caso di collegamento ad aspiratori meccanici verificare frequentemente la connessione.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
EL		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08033609528493
Basic UDI-DI: 803360952CANNULEG9
Reference / catalog number: KIT 007
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: Aspiration cannula
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.

A06010103CANNULAS AND TIPS FOR ASPIRATION AND IRRIGATION, SINGLE-USE

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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