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Guedel Airway

EUDAMED

Class I (EU MDR)

Ref GUA

by Disposafe Health & Lifecare Limited

Identity

Trade Name
Guedel Airway EUDAMED
Device Name
Guedal Airway EUDAMED
Model / Reference
GUA EUDAMED

Identifiers

Primary DI / UDI-DI
GUA-3 EUDAMED
Basic UDI-DI
++G401GUARJ EUDAMED
EMDN Code
R010102 GUEDEL AIRWAY TUBES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Guedel Airway by Disposafe Health & Lifecare Limited — Class I — 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
IN-MF-000020265
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED c5707c7d-4acc-4cf3-b2aa-57d13aad194d 61 fields · synced Jul 14, 2026