Skip to content

Lma Airway Management IPN929256

by Teleflex Incorporated

Ref 136075

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08019020000000000000288LA Basic UDI-DI 14026704934765UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14026704934765 UDI-DI Date3 Aug 2026ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
LMA Fastrach ETT Single Use EUDAMED
Lma Airway Management GUDID
Generic Name
Basic endotracheal tube, single-use
Device Name
LMA Fastrach ETT SU
Model / Ref / Catalog
136075, IPN929256
Primary DI / UDI-DI
14026704934765
Basic UDI-DI
08019020000000000000288LA
FDA Product Code
BTR
EMDN Code
R01030202 Endotracheal tubes, cuffed, reinforced
GMDN Term
Basic endotracheal tube, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
868.5730
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Outer Diameter — 10.3 Millimeter
Lumen/Inner Diameter — 7.5 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
136075
GUDID
IPN929256
Device ClassEUDAMED
Class IIa
GUDID
Class II

Other devices from Teleflex Incorporated

See all devices from Teleflex Incorporated →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (20)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No