← Back to catalogue

Graftmaster

FDA UDI

Class Unclassified (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
Graftmaster FDA UDI
Generic Name
Bare-metal coronary artery stent FDA UDI
Device Name
GRAFTMASTER Coronary Stent Graft System 4.80 mm x 26 mm / Rapid-Exchange FDA UDI
Model / Reference
1012584-26 FDA UDI
Description
GRAFTMASTER Coronary Stent Graft System 4.80 mm x 26 mm / Rapid-Exchange FDA UDI

Identifiers

Catalog Number
1012584-26 FDA UDI
Primary DI / UDI-DI
08717648176524 FDA UDI
FDA Product Code
NIV FDA UDI
DYG FDA UDI
MAF FDA UDI
GMDN Term
Bare-metal coronary artery stent FDA UDI

Classification

Device Class
Unclassified FDA UDI
Regulation Number
870.1240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bare-metal coronary artery stent

Graftmaster by Abbott Vascular — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal coronary artery stent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Abbott Vascular

Sources (1)

  • FDA UDI a22a4754-4428-427a-9eb6-a09d9f597ca1 36 fields · synced May 30, 2026