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Axiom® 503NS

by Axiom Medical, Incorporated

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 NumberM665503NS0 UDI-DI Date13 Nov 2020ListedStatusListed 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  • Withdrawn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
Axiom®
Generic Name
Suction/irrigation tubing, single-use
Model / Reference
503NS
Primary DI / UDI-DI
M665503NS0
FDA Product Code
GAZ
GMDN Term
Suction/irrigation tubing, single-use
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Lumen/Inner Diameter — 0.078 Inch
Outer Diameter — 0.125 Inch
Length — 50 Feet

Related devices

Category: Suction/irrigation tubing, single-use

Other devices from Axiom Medical, Incorporated

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Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration 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
  • Manufacturing Date: No