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Multi-Link Mini Vision

FDA UDI

Class III (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
MULTI-LINK MINI VISION FDA UDI
Generic Name
Bare-metal coronary artery stent FDA UDI
Device Name
MULTI-LINK MINI VISION Coronary Stent and Stent Delivery System 2.25 mm x 23 mm / Rapid-Exchange FDA UDI
Model / Reference
1007822-23 FDA UDI
Description
MULTI-LINK MINI VISION Coronary Stent and Stent Delivery System 2.25 mm x 23 mm / Rapid-Exchange FDA UDI

Identifiers

Catalog Number
1007822-23 FDA UDI
Primary DI / UDI-DI
08717648049477 FDA UDI
FDA Product Code
MAF FDA UDI
GMDN Term
Bare-metal coronary artery stent FDA UDI

Classification

Device Class
Class III 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

Multi-Link Mini Vision by Abbott Vascular — Class III — 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

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Manufacturer

Manufacturer
Abbott Vascular

Sources (1)

  • FDA UDI 83c52ace-44d5-4a1e-b371-22e0bb1d464c 37 fields · synced Jun 8, 2026