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Altech

EUDAMED

Class IIa (EU MDR)

Ref AL-1222-060.V004

by Meditera Tıbbi Malzeme Sanayi ve Ticaret A.Ş.

Identity

Trade Name
ALTECH EUDAMED
Device Name
DOUBLE LINE/DOUBLE LUMEN BREATHING CIRCUIT (Non-Sterile) EUDAMED
Model / Reference
AL-1222-060.V004 EUDAMED

Identifiers

Primary DI / UDI-DI
+M485AL1222060V0040U EUDAMED
Basic UDI-DI
++M485BCNS0010ZU EUDAMED
Direct Marketing DI
+M485AL1222060V0040U EUDAMED
EMDN Code
R02010102 BREATHING CIRCUITS, WITH WATER TRAP 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

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

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 e0fd35cb-cc6e-4115-ab53-6179a7959996 61 fields · synced Jun 18, 2026