Skip to content

MSI Precision Specialty Instruments DTL-7.50

by Med Saver, Inc.

MSI Precision Specialty Instruments DTL-7.50 is a Class I device made by Med Saver, Inc., listed in FDA GUDID since 15 Aug 2024 (UDI-DI 00194613045852), 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 Number00194613045852 UDI-DI Date15 Aug 2024ListedStatusListed 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  • Withdrawn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
Corneal punch set
Model / reference
DTL-7.50
Primary DI / UDI-DI
00194613045852
FDA product code
HRH
GMDN term
Corneal punch set
Device class
Class I
Regulation number
886.4350
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Corneal punch set

Similar devices in this category

Other devices filed under Corneal punch set.

Other devices from Med Saver, Inc.

See all devices from Med Saver, Inc. →

Properties

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