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Vermed ELD K140-1020

by Graphic Controls Acquisition Corp

Vermed ELD K140-1020 (10784107) is a Class I device made by Graphic Controls Acquisition Corp, listed in FDA GUDID since 23 Sep 2018 (UDI-DI 00009336000289), 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 Number00009336000289 UDI-DI Date23 Sep 2018ListedStatusListed 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  • Withdrawn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
Vermed
Generic name
Electrocardiographic recording paper
Model / Ref / Catalog
ELD K140-1020, 10784107
Primary DI / UDI-DI
00009336000289
FDA product code
DSF
GMDN term
Electrocardiographic recording paper
Device class
Class I
Regulation number
870.2810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrocardiographic recording paper

Other devices from Graphic Controls Acquisition Corp

See all devices from Graphic Controls Acquisition Corp →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)