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Duravent 11000-03

by Andreas Fahl Medizintechnik-Vertrieb GmbH

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04051948004519 UDI-DI Date17 Sep 2015ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Duravent
Generic Name
Tracheostomy tube, non-reinforced, non-customized, reusable
Model / Reference
11000-03
Primary DI / UDI-DI
04051948004519
FDA Product Code
BTR, BTO, JOH
GMDN Term
Tracheostomy tube, non-reinforced, non-customized, reusable
Device Class
Class II
Regulation Number
868.5730, 868.5800
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Safe

Other devices from Andreas Fahl Medizintechnik-Vertrieb GmbH

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Properties

  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No