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Kendall

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Electrode/transducer strap, single-use FDA UDI
Device Name
Tab Belt,Pink and Blue FDA UDI
Model / Reference
40000009 FDA UDI
Description
Tab Belt,Pink and Blue FDA UDI

Identifiers

Catalog Number
40000009 FDA UDI
Primary DI / UDI-DI
20884527005533 FDA UDI
FDA Product Code
FSD FDA UDI
GMDN Term
Electrode/transducer strap, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5160 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

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Length — 36 Inch FDA UDI
Width — 1.5 Inch FDA UDI

Category: Electrode/transducer strap, single-use

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

Similar devices

Also classified as Electrode/transducer strap, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 4820734d-5665-497f-b328-b84f032ba7b4 37 fields · synced Jun 8, 2026