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ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 37 FR

EUDAMED

Class IIa (EU MDR)

Ref 4011-37/LModel ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 37 FRModel ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen)

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

Identity

Trade Name
ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 37 FR EUDAMED
Device Name
ULTRAMED ENDOTRACHEAL TUBE EUDAMED
Model / Reference
ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) Left 37 FR EUDAMED
4011-37/L EUDAMED
ULTRAMED ENDOTRACHEAL TUBE (Double - Lumen) EUDAMED

Identifiers

Primary DI / UDI-DI
06223004254178 EUDAMED
Basic UDI-DI
B-06223004254178 EUDAMED
6223004254011PC 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 37 FR by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E) — Class IIa — MDR, MDD — 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/MDR

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED 406671b8-7c1b-4529-925b-7c9a44e54970 61 fields · synced Oct 7, 2026
  • EUDAMED fb6019d0-6de8-4b9e-9f03-32e94878882f 61 fields · synced May 16, 2026