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Hummingbird Tympanostomy Tube System 05-1001-652

by Preceptis Medical

Listed FDA GUDID listing, no authorization on record

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00853386007060 UDI-DI Date12 Apr 2021ListedStatusListed GUDID: 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  • Withdrawn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
Hummingbird Tympanostomy Tube System
Generic Name
Tympanostomy tube
Model / Ref / Catalog
05-1001-652
Primary DI / UDI-DI
00853386007060
FDA Product Code
ETD
GMDN Term
Tympanostomy tube
Device Class
Class II
Regulation Number
874.3880
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tympanostomy tube

Other devices from Preceptis Medical

See all devices from Preceptis Medical →

Properties

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

Other properties (8)

  • 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