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Cps Aim™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical, Inc.

Identity

Trade Name
CPS AIM™ FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
Slittable Inner Catheter (Subselector) FDA UDI
Model / Reference
DS2M055 FDA UDI
Description
Slittable Inner Catheter (Subselector) FDA UDI

Identifiers

Catalog Number
DS2M055 FDA UDI
Primary DI / UDI-DI
05414734509541 FDA UDI
510(k) Number
K142235 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Vascular guide-catheter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 59 Centimeter FDA UDI
Catheter Gauge — 8 French FDA UDI
Length — 238.7000 Centimeter FDA UDI

Category: Vascular guide-catheter, single-use

Cps Aim™ by St. Jude Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular guide-catheter, single-use.

Cleared under the same submission

K142235 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
St. Jude Medical, Inc.

Sources (1)

  • FDA UDI 8ad59a5f-b0e5-4507-af65-0463d3c39f17 38 fields · synced Jun 6, 2026