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Tri-Electrode Surface EMG 730-003

by SRS Medical Systems, Inc.

Tri-Electrode Surface EMG 730-003 is a Class II device made by SRS Medical Systems, Inc., listed in FDA GUDID since 4 Mar 2026 (UDI-DI 00890477000395), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00890477000395 UDI-DI Date4 Mar 2026ListedStatusListed 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  • Withdrawn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
Tri-Electrode Surface EMG
Generic name
Cystometer
Model / reference
730-003
Primary DI / UDI-DI
00890477000395
FDA product code
EXQ
GMDN term
Cystometer
Device class
Class II
Regulation number
876.1620
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EXQ (Cystometer, Electrical Recording).

Other devices from SRS Medical Systems, Inc.

See all devices from SRS Medical Systems, Inc. →

Properties

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