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Synergetics 70025E

by Synergetics USA, Inc.

Synergetics 70025E is a Class II device made by Synergetics USA, Inc., listed in FDA GUDID since 22 Jul 2016 (UDI-DI 20841305108480), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20841305108480 UDI-DI Date22 Jul 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  • Withdrawn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
Synergetics
Generic name
Ophthalmic surgical procedure kit, non-medicated, single-use
Model / Ref / Catalog
70025E
Primary DI / UDI-DI
20841305108480
FDA product code
HQE
GMDN term
Ophthalmic surgical procedure kit, non-medicated, single-use
Device class
Class II
Regulation number
886.4150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic surgical procedure kit, non-medicated, single-use

Similar devices in this category

Other devices filed under Ophthalmic surgical procedure kit, non-medicated, single-use.

Other devices from Synergetics, Inc.

See all devices from Synergetics, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)