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NIRxcell CoCr Coronary Stent on RX System

FDA UDI

Class III (US FDA UDI)

by Medinol Ltd.

Identity

Trade Name
NIRxcell CoCr Coronary Stent on RX System FDA UDI
Generic Name
Bare-metal coronary artery stent FDA UDI
Model / Reference
NXL27520US FDA UDI

Identifiers

Primary DI / UDI-DI
07290107010825 FDA UDI
PMA Number
P110004 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

Dimensions & Sizes

Size
Length — 20 Millimeter FDA UDI
Outer Diameter — 2.75 Millimeter FDA UDI

Category: Bare-metal coronary artery stent

NIRxcell CoCr Coronary Stent on RX System by Medinol Ltd. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal coronary artery stent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medinol Ltd.

Sources (1)

  • FDA UDI 8c7bd4c3-7ad8-4f14-8a00-ea03f894b4f9 36 fields · synced May 30, 2026