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ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Cuffed Size 8.5

EUDAMED

Class IIa (EU MDR)

Ref 4009-8.5/PNModel ULTRAMED ENDOTRACHEAL TUBE Preformed NasalModel ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Cuffed Size 8.5

by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)

Identity

Trade Name
ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Cuffed Size 8.5 EUDAMED
Device Name
ULTRAMED ENDOTRACHEAL TUBE EUDAMED
ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Cuffed EUDAMED
Model / Reference
ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal EUDAMED
4009-8.5/PN EUDAMED
ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Cuffed Size 8.5 EUDAMED

Identifiers

Primary DI / UDI-DI
06223004254352 EUDAMED
Basic UDI-DI
622300425ETT4010/PNN5 EUDAMED
B-06223004254352 EUDAMED
EMDN Code
R01030201 ENDOTRACHEAL TUBES, CUFFED, NOT REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Bulgaria 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

Category: Basic endotracheal tube, single-use

ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Cuffed Size 8.5 by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E) — Class IIa — MDD, MDR — listed in EUDAMED

Similar devices

Also classified as Basic endotracheal tube, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
EG-MF-000038562
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 48f71919-d790-4c4f-8174-0eb2223f1503 61 fields · synced Oct 6, 2026
  • EUDAMED cbd0b3c4-c488-4e63-9f00-233f9fe9486f 61 fields · synced May 19, 2026