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MSI Precision Specialty Instruments DUO-06

by Med Saver, 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 Number00194613036768 UDI-DI Date1 Aug 2025ListedStatusListed 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  • Withdrawn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
MSI Precision Specialty Instruments
Generic Name
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Model / Reference
DUO-06
Primary DI / UDI-DI
00194613036768
FDA Product Code
HNR
GMDN Term
Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Other devices from Med Saver, Inc.

See all devices from Med Saver, 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