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Kendall

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Radiolucent electrocardiographic lead FDA UDI
Device Name
DL Disposable Lead Set 5 Lead, Radiolucent FDA UDI
Model / Reference
33136RT36 FDA UDI
Description
DL Disposable Lead Set 5 Lead, Radiolucent FDA UDI

Identifiers

Catalog Number
33136RT36 FDA UDI
Primary DI / UDI-DI
10884521212640 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Radiolucent electrocardiographic lead 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

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

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 — 3 Feet FDA UDI

Category: Radiolucent electrocardiographic lead

Kendall by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiolucent electrocardiographic lead.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI ed0ee4b0-a20d-4528-a8b5-62f91cbc8db6 37 fields · synced May 30, 2026