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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 switching adaptor FDA UDI
Device Name
Finished product, non-sterile, Kendall DL, 3 or 5 Lead, GE CARESCAPE ONE only Product code 33523 FDA UDI
Model / Reference
33523 FDA UDI
Description
Finished product, non-sterile, Kendall DL, 3 or 5 Lead, GE CARESCAPE ONE only Product code 33523 FDA UDI

Identifiers

Catalog Number
33523 FDA UDI
Primary DI / UDI-DI
10192253065466 FDA UDI
FDA Product Code
IKD FDA UDI
GMDN Term
Electrocardiographic lead switching adaptor 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead switching adaptor

A finished product, non-sterile Kendall DL, 3 or 5 Lead, GE CARESCAPE ONE only Product code 33523.

Similar devices

Also classified as Electrocardiographic lead switching adaptor.

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 c431c6ff-7a72-44f6-9991-14973903f98c 34 fields · synced Jul 12, 2026