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Morton

EUDAMED

Class IIa (EU MDR)

Ref MN 102-03 PE

by Morton Medikal San ve Tic A.Ş.

Identity

Trade Name
MORTON EUDAMED
Device Name
Breathing Circuit Adult with one water trap, PE 1.50 m EUDAMED
Model / Reference
MN 102-03 PE EUDAMED

Identifiers

Primary DI / UDI-DI
D-8698940543910JN EUDAMED
Basic UDI-DI
B-8698940543910JN EUDAMED
EMDN Code
R02010102 BREATHING CIRCUITS, WITH WATER TRAP EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Bulgaria 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 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 825f4a61-7394-4330-b226-4e34a0fbc4df 61 fields · synced Jun 20, 2026