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SentioMMG 2007

by Innovative Surgical Solutions LLC

Listed FDA GUDID listing, not in commercial distribution

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00853926005020 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
SentioMMG
Generic Name
Analytical non-scalp cutaneous electrode
Model / Ref / Catalog
2007
Primary DI / UDI-DI
00853926005020
FDA Product Code
PDQ
GMDN Term
Analytical non-scalp cutaneous electrode
Device Class
Class II
Regulation Number
874.1820
GUDID distribution status
Not in Commercial Distribution

Other devices from Innovative Surgical Solutions, LLC (Iss)

  • Neuralmas

    Class II

  • Sentio Mmg

    Class II

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: 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
  • Manufacturing Date: No