Cxi

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name: CXI FDA UDI
Generic Name: Angiographic catheter, single-use FDA UDI
Device Name: CXI Support Catheter FDA UDI
Model / Reference: G18367 FDA UDI
Description: CXI Support Catheter FDA UDI

Identifiers

Catalog Number: CXI-2.6-18-65-P-NS-0 FDA UDI
Primary DI / UDI-DI: 00827002183674 FDA UDI
FDA Product Code: KRA FDA UDI
GMDN Term: Angiographic catheter, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1210 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Angiographic catheter, single-use

Cxi by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

INFINITI — Cordis US Corp. · Class II
Performa® — Merit Medical Systems, Inc. · Class II
Performa® — Merit Medical Systems, Inc. · Class II
Performa® — Merit Medical Systems, Inc. · Class II
ConcierGE Guiding Excellence™ — Merit Medical Systems, Inc. · Class II
INFINITI — Cordis US Corp. · Class II
SUPER TORQUE — Cordis Corp. · Class II
Performa® — Merit Medical Systems, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Cook Incorporated

Sources (1)

FDA UDI 8ddd1a39-3143-4a22-bd2e-74a7bed166f1 36 fields · synced Jun 8, 2026