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Guedel Airway

EUDAMED

Class I (EU MDR)

Ref 1603-0090

by Fortune Medical Instrument Corp.

Identity

Trade Name
Guedel Airway EUDAMED
Device Name
Guedel Airway EUDAMED
Model / Reference
1603-0090 EUDAMED

Identifiers

Primary DI / UDI-DI
34711182604562 EUDAMED
Basic UDI-DI
B-34711182604562 EUDAMED
EMDN Code
R010102 GUEDEL AIRWAY TUBES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Guedel Airway by Fortune Medical Instrument Corp. — Class I — 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
TW-MF-000009221
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED ce2fa03f-9861-4303-828f-f2aab84dcf94 61 fields · synced Jul 10, 2026