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Morton Medical

EUDAMED

Class IIa (EU MDR)

Ref MN 100-01 PE

by Morton Medikal San ve Tic A.Ş.

Identity

Trade Name
MORTON MEDICAL EUDAMED
Device Name
ANESTHESIA CIRCUIT EUDAMED
Model / Reference
MN 100-01 PE EUDAMED

Identifiers

Primary DI / UDI-DI
D-8698940543514JA EUDAMED
Basic UDI-DI
B-8698940543514JA EUDAMED
EMDN Code
R02010199 STANDARD BREATHING CIRCUITS - OTHER 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Morton Medical by Morton Medikal San ve Tic A.Ş. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000020441

Sources (1)

  • EUDAMED e94b8dde-575c-448f-bc79-79e8efc6b3c4 61 fields · synced Jun 19, 2026