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Kendall

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Patient monitoring system module rack FDA UDI
Device Name
Cable and Lead Wire Accessory, Adapter Clip FDA UDI
Model / Reference
22660A FDA UDI
Description
Cable and Lead Wire Accessory, Adapter Clip FDA UDI

Identifiers

Catalog Number
22660A FDA UDI
Primary DI / UDI-DI
20884521148342 FDA UDI
510(k) Number
K942321 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Patient monitoring system module rack FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient monitoring system module rack

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

Similar devices

Also classified as Patient monitoring system module rack.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 1d344379-b4b3-42b7-b0c7-3cc10e0af0e4 37 fields · synced May 30, 2026