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Graftmaster 1012584-26

by Abbott Vascular

Graftmaster 1012584-26 is a device classified as Unclassified made by Abbott Vascular, listed in FDA GUDID since 21 Nov 2014 (UDI-DI 08717648176524), 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 Number08717648176524 UDI-DI Date21 Nov 2014ListedStatusListed 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  • Withdrawn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
Graftmaster
Generic name
Bare-metal coronary artery stent
Model / Ref / Catalog
1012584-26
Primary DI / UDI-DI
08717648176524
FDA product code
NIV, DYG, MAF
GMDN term
Bare-metal coronary artery stent
Device class
Unclassified
Regulation number
870.1240
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Bare-metal coronary artery stent

Other devices from Abbott Vascular

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)