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CorPath Interventional Cockpit

FDA UDI

Class I (US FDA UDI)

by Corindus, Inc.

Identity

Trade Name
CorPath Interventional Cockpit FDA UDI
Generic Name
Radiation shielding panel, portable/mobile FDA UDI
Model / Reference
101 FDA UDI

Identifiers

Catalog Number
101 FDA UDI
Primary DI / UDI-DI
00816280021013 FDA UDI
FDA Product Code
IWX FDA UDI
GMDN Term
Radiation shielding panel, portable/mobile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiation shielding panel, portable/mobile

CorPath Interventional Cockpit by Corindus, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation shielding panel, portable/mobile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corindus, Inc.

Sources (1)

  • FDA UDI dcf49c0c-7467-4df6-a986-5192bea130a7 34 fields · synced May 30, 2026