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S.m.a.r.t. Radianz

FDA UDI

Class III (US FDA UDI)

by Cordis Corp.

Identity

Trade Name
S.M.A.R.T. RADIANZ FDA UDI
Generic Name
Peripheral artery stent, bare-metal FDA UDI
Device Name
S.M.A.R.T. RADIANZ Vascular Stent System 8x60mm 190CM FDA UDI
Model / Reference
SR08060XL FDA UDI
Description
S.M.A.R.T. RADIANZ Vascular Stent System 8x60mm 190CM FDA UDI

Identifiers

Catalog Number
SR08060XL FDA UDI
Primary DI / UDI-DI
20705032082485 FDA UDI
PMA Number
P020036 FDA UDI
P120002 FDA UDI
FDA Product Code
NIO FDA UDI
NIP FDA UDI
GMDN Term
Peripheral artery stent, bare-metal 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: Peripheral artery stent, bare-metal

S.m.a.r.t. Radianz by Cordis Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral artery stent, bare-metal.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cordis Corp.

Sources (1)

  • FDA UDI eba57ea3-7d03-4d3e-99b6-b9076f5ba659 36 fields · synced Jun 6, 2026