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Airliquide

EUDAMED

Class IIa (EU MDR)

Ref AL-08023.V013

by Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş.

Identity

Trade Name
Airliquide EUDAMED
Device Name
Bacterial Viral Filter EUDAMED
Model / Reference
AL-08023.V013 EUDAMED

Identifiers

Primary DI / UDI-DI
+M485AL08023V0131V EUDAMED
Basic UDI-DI
++M485FLTNS080HW EUDAMED
Direct Marketing DI
+M485AL08023V0131V EUDAMED
EMDN Code
R040101 ANTIBACTERIAL AND ANTIVIRAL RESPIRATORY FILTERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Secretion suction kit

Airliquide by Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Secretion suction kit.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TR-MF-000014943

Sources (1)

  • EUDAMED 686d720f-14df-4200-9fc0-ecf9870523af 61 fields · synced Jun 18, 2026