Skip to content

Single Use Professional OPR002

by Eakin Surgical Limited 2 variants

Single Use Professional OPR002 is a Class II device made by Eakin Surgical Limited, listed in FDA GUDID since 9 Jan 2024 (UDI-DI 05055299101575), 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 Number05055299101575 UDI-DI Date9 Jan 2024ListedStatusListed 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  • Withdrawn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
OPR002
Primary DI / UDI-DI
05055299101575
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

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)