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Ruschelit Safety ClearTracheal Tube, Oral/Nasal

EUDAMED

Class IIa (EU MDR)

Ref 100382-000030

by Teleflex Medical Sdn. Bhd.

Identity

Trade Name
Ruschelit Safety ClearTracheal Tube, Oral/Nasal EUDAMED
Device Name
TRACHEAL TUBE EUDAMED
Model / Reference
100382-000030 EUDAMED

Identifiers

Primary DI / UDI-DI
14026704333155 EUDAMED
Basic UDI-DI
B-14026704333155 EUDAMED
EMDN Code
R01030101 ENDOTRACHEAL TUBES, CUFFLESS, NOT REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Ruschelit Safety ClearTracheal Tube, Oral/Nasal by Teleflex Medical Sdn. Bhd. — 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
MY-MF-000024692
Authorised Representative
Teleflex Medical IE-AR-000015869

Sources (1)

  • EUDAMED 261b5dc3-cc6b-4989-af36-2b1838ce8585 61 fields · synced Jul 8, 2026