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MSI Precision Specialty Instruments 108-I19-01A

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 Number00194613084646 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  • Withdrawn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
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
Model / Reference
108-I19-01A
Primary DI / UDI-DI
00194613084646
FDA Product Code
GEI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Other devices from Med Saver, Inc.

See all devices from Med Saver, Inc. →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

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