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Super Torque

FDA UDI

Class II (US FDA UDI)

by Cordis Corp.

Identity

Trade Name
SUPER TORQUE FDA UDI
Generic Name
Angiographic catheter, single-use FDA UDI
Device Name
CP 5.2F ST+ JL5, JR4, PIG. FDA UDI
Model / Reference
CP0260 FDA UDI
Description
CP 5.2F ST+ JL5, JR4, PIG. FDA UDI

Identifiers

Catalog Number
CP0260 FDA UDI
Primary DI / UDI-DI
10705032026192 FDA UDI
510(k) Number
K914007 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Angiographic catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Angiographic catheter, single-use

Super Torque by Cordis Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic catheter, single-use.

Cleared under the same submission

K914007 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cordis Corp.

Sources (1)

  • FDA UDI d022b759-2bb6-4200-93c2-eff56e68be9c 35 fields · synced May 30, 2026