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Catalano Lacrimal Intubation Set 16-2590

by Sontec Instruments, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896116955 UDI-DI Date25 Mar 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Catalano Lacrimal Intubation Set
Generic Name
Ophthalmic surgical probe, reusable
Model / Ref / Catalog
16-2590
Primary DI / UDI-DI
00192896116955
FDA Product Code
HNL
GMDN Term
Ophthalmic surgical probe, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilization Method
Dry Heat Sterilization
Size
Outer Diameter — 0.7 Millimeter

Related devices

Category: Ophthalmic surgical probe, reusable

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No