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MSI Precision Specialty Instruments 1770-SAMPLE

by Med Saver, Inc.

MSI Precision Specialty Instruments 1770-SAMPLE is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 1 Aug 2025 (UDI-DI 00194613118945), 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 Number00194613118945 UDI-DI Date1 Aug 2025ListedStatusListed 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  • Withdrawn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
MSI Precision Specialty Instruments
Generic name
Radiation/mechanical corneal shield, reusable
Model / reference
1770-SAMPLE
Primary DI / UDI-DI
00194613118945
FDA product code
HOY
GMDN term
Radiation/mechanical corneal shield, reusable
Device class
Class I
Regulation number
886.4750
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Radiation/mechanical corneal shield, reusable

Similar devices in this category

Other devices filed under Radiation/mechanical corneal shield, reusable.

Other devices from Med Saver, Inc.

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)