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Single Use Professional S055

by Eakin Surgical Limited

Single Use Professional S055 is a Class II device made by Eakin Surgical Limited, listed in FDA GUDID since 9 Aug 2016 (UDI-DI 05055299101216), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05055299101216 UDI-DI Date9 Aug 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Single Use Professional
Generic name
Surgical irrigation/aspiration cannula, non-illuminating, single-use
Model / Ref / Catalog
S055
Primary DI / UDI-DI
05055299101216
FDA product code
GCX
GMDN term
Surgical irrigation/aspiration cannula, non-illuminating, single-use
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 6 French
Length — 13 Centimeter

Related devices

Category: Surgical irrigation/aspiration cannula, non-illuminating, single-use

Similar devices

Other devices filed under FDA product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered).

Other devices from Eakin Surgical Limited

See all devices from Eakin Surgical Limited →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)