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ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 39 FR

EUDAMED

Class IIa (EU MDR)

Ref 4011-39/LModel ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Model ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 39 FR

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

Identity

Trade Name
ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 39 FR EUDAMED
Device Name
ULTRAMED ENDOTRACHEAL TUBE EUDAMED
Model / Reference
ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) EUDAMED
4011-39/L EUDAMED
ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 39 FR EUDAMED

Identifiers

Primary DI / UDI-DI
06223004254185 EUDAMED
Basic UDI-DI
6223004254011PC EUDAMED
B-06223004254185 EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa 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: Reinforced endotracheal tube, single-use

ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 39 FR 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 Reinforced 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 e6083cf8-bfb2-467f-a11d-a1d63cd1aff9 61 fields · synced Oct 8, 2026
  • EUDAMED 50a242e9-406d-4f39-813b-c1dec2361bb5 61 fields · synced May 18, 2026