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Kendall

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Kendall FDA UDI
Generic Name
Electrocardiographic lead set, single-use FDA UDI
Device Name
Kendall DL ECG Direct Connect Telemetry Lead Wires for Philips MX40 Monitors, 6-Lead, Single Patient Use, Masimo SpO2 FDA UDI
Model / Reference
33152 FDA UDI
Description
Kendall DL ECG Direct Connect Telemetry Lead Wires for Philips MX40 Monitors, 6-Lead, Single Patient Use, Masimo SpO2 FDA UDI

Identifiers

Catalog Number
33152 FDA UDI
Primary DI / UDI-DI
10192253063196 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrocardiographic lead set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.1175 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 3 Feet FDA UDI

Category: Electrocardiographic lead set, single-use

Kendall by Cardinal Health 200, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI 6e7b2116-923f-4380-ad2c-2a46d412891f 35 fields · synced Jun 8, 2026