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Poole 9035070

by Conmed Corporation

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 Number20653405014956 UDI-DI Date24 Mar 2026ListedStatusListed 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  • Withdrawn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
Poole
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use
Model / Ref / Catalog
9035070
Primary DI / UDI-DI
20653405014956
FDA Product Code
GCX
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Length — 10 Feet
Length — 3 Meter

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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

Other properties (9)

  • Sterile: 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