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Silicone Endotracheal Tube

EUDAMED

Class IIa (EU MDR)

Ref 1555-0080

by Fortune Medical Instrument Corp.

Identity

Trade Name
Silicone Endotracheal Tube EUDAMED
Device Name
Silicone Endotracheal Tube EUDAMED
Model / Reference
1555-0080 EUDAMED

Identifiers

Primary DI / UDI-DI
14710961930911 EUDAMED
Basic UDI-DI
B-14710961930911 EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Romania EUDAMED

Clinical & Handling

Sterile

Yes

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

Category: Reinforced endotracheal tube, single-use

Silicone Endotracheal Tube by Fortune Medical Instrument Corp. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Reinforced endotracheal tube, single-use.

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 83d9c249-56e9-4ffc-acce-0ba6c67ccec9 61 fields · synced Jun 19, 2026