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Xact™

FDA UDI

Class III (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
XACT™ FDA UDI
Generic Name
Bare-metal carotid artery stent FDA UDI
Device Name
XACT™ Transcarotid Stent System 8.0 mm x 30 mm Straight FDA UDI
Model / Reference
83023-01 FDA UDI
Description
XACT™ Transcarotid Stent System 8.0 mm x 30 mm Straight FDA UDI

Identifiers

Catalog Number
83023-01 FDA UDI
Primary DI / UDI-DI
08717648356735 FDA UDI
FDA Product Code
NIM FDA UDI
GMDN Term
Bare-metal carotid 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 carotid artery stent

Xact™ by Abbott Vascular — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal carotid 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 c15ab22e-7d58-47cc-9477-1b313c10c1ef 36 fields · synced May 31, 2026