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Vermed V8930

by Graphic Controls Acquisition Corp

Vermed V8930 is a Class II device made by Graphic Controls Acquisition Corp, listed in FDA GUDID since 12 Jul 2017 (UDI-DI 10009336008442), not in commercial distribution (GUDID) as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10009336008442 UDI-DI Date12 Jul 2017ListedStatusListed GUDID: not 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  • Withdrawn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
Vermed
Generic name
Electrocardiographic electrode, single-use
Model / Ref / Catalog
V8930
Primary DI / UDI-DI
10009336008442
FDA product code
DRX
GMDN term
Electrocardiographic electrode, single-use
Device class
Class II
Regulation number
870.2360
GUDID distribution status
Not in Commercial Distribution

Other devices from Graphic Controls Acquisition Corp

See all devices from Graphic Controls Acquisition Corp →

Properties

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