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ENT-single-use suction tubes, angled 3013020

by Spiggle & Theis Medizintechnik GmbH

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04250676716880 UDI-DI Date29 Sep 2025ListedStatusListed 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  • Withdrawn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
ENT-single-use suction tubes, angled
Generic Name
Suction/irrigation tubing, single-use
Model / Ref / Catalog
3013020
Description
transparent, Luer-Lock 130 x 2.0 mm, sterile, box of 50
Primary DI / UDI-DI
04250676716880
FDA Product Code
BYY
GMDN Term
Suction/irrigation tubing, single-use
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution

Other devices from Spiggle & Theis Medizintechnik GmbH

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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