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Synergetics 30.35

by Synergetics USA, Inc.

Synergetics 30.35 is a Class I device made by Synergetics USA, Inc., listed in FDA GUDID since 30 May 2020 (UDI-DI 10841305111919), 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 Number10841305111919 UDI-DI Date30 May 2020ListedStatusListed 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  • Withdrawn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 irrigation/infusion/aspiration cannula, non-illuminating, single-use
Model / Ref / Catalog
30.35
Primary DI / UDI-DI
10841305111919
FDA product code
HMX
GMDN term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution

Related devices

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

Similar devices in this category

Other devices filed under Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use.

Other devices from Synergetics, Inc.

See all devices from Synergetics, Inc. →

Properties

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