EUDAMED last updated this device on Aug 5, 2026

CORTEX ASPIRATOR

B-08681092050597

On the marketClass IIa

Applicable legislation: —
Organization name: MMT MERAN MEDİKAL TEKNOLOJİ KOLL. ŞTİ. Ahmet Cemil Baytaş ve Fatma Baytaş
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 →: 08681092050597
Reference / catalog number: CORTEX ASPIRATOR

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

CORTEX ASPIRATOR is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by MMT MERAN MEDİKAL TEKNOLOJİ KOLL. ŞTİ. Ahmet Cemil Baytaş ve Fatma Baytaş. Placed on the EU market in Türkiye. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: CORTEX ASPIRATOR
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 →: 08681092050597
Basic 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 →: B-08681092050597
Reference / catalog number: CORTEX ASPIRATOR
UDI 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 →: GS1

Classification

Risk category: Class IIa
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 0,50x22mm (25gx7/8in)

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08681092050597

EMDN nomenclature code(s)

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

Q021101OCCULAR IRRIGATION AND ASPIRATION CANNULAS, SINGLE-USE

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Türkiye; available across 8 countries total.

Country	On market since	Until
TürkiyePrimary placement	Apr 17, 2020	Still on market
EL	Apr 17, 2020	Still on market
France	Apr 17, 2020	Still on market
Ireland	Apr 17, 2020	Still on market
Italy	Apr 17, 2020	Still on market
Latvia	Apr 17, 2020	Still on market
Malta	Apr 17, 2020	Still on market
Poland	Apr 17, 2020	Still on market

Related searches

Class IIa medical devices in EUDAMED

Device identification

Trade name: CORTEX ASPIRATOR
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 →: 08681092050597
Basic 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 →: B-08681092050597
Reference / catalog number: CORTEX ASPIRATOR
UDI 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 →: GS1

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Certificates

No certificates registered for this manufacturer.

Market distribution

Primary placement in Türkiye; available across 8 countries total.

Country	On market since	Until
TürkiyePrimary placement	Apr 17, 2020	Still on market
EL	Apr 17, 2020	Still on market
France	Apr 17, 2020	Still on market
Ireland	Apr 17, 2020	Still on market
Italy	Apr 17, 2020	Still on market
Latvia	Apr 17, 2020	Still on market
Malta	Apr 17, 2020	Still on market
Poland	Apr 17, 2020	Still on market

CORTEX ASPIRATOR

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Legacy certificates

Certificates covering this device

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Market distribution

Related searches

Manufacturer information

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Certificates

Certificates covering this device

Legacy certificates