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Single Use Professional S010

by Eakin Surgical Limited

Single Use Professional S010 is a Class II device made by Eakin Surgical Limited, listed in FDA GUDID since 9 Aug 2016 (UDI-DI 05055299100899), 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 Number05055299100899 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  • Withdrawn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/emergency suction cannula, non-illuminating, single-use
Model / Ref / Catalog
S010
Primary DI / UDI-DI
05055299100899
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

Related devices

Category: Surgical/emergency suction cannula, non-illuminating, single-use

Similar devices in this category

Other devices filed under Surgical/emergency suction cannula, non-illuminating, single-use.

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Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)