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Roadsaver Carotid Atery Stent

FDA UDI

Class III (US FDA UDI)

by Microvention Inc.

Identity

Trade Name
Roadsaver Carotid Atery Stent FDA UDI
Generic Name
Bare-metal carotid artery stent FDA UDI
Device Name
Roadsaver Carotid Atery Stent FDA UDI
Model / Reference
RDS-0718-143RX-MVI FDA UDI
Description
Roadsaver Carotid Atery Stent FDA UDI

Identifiers

Catalog Number
RDS-0718-143RX FDA UDI
Primary DI / UDI-DI
00811425024669 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Bare-metal carotid artery stent

Roadsaver Carotid Atery Stent by Microvention Inc. — 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
Microvention Inc.

Sources (1)

  • FDA UDI 0c210140-ef0c-41cf-b9ea-2c3fdfba5593 36 fields · synced May 31, 2026