Kendall

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name: Kendall FDA UDI
Generic Name: Electrocardiographic recording paper FDA UDI
Device Name: Medical Recording Chart Paper FDA UDI
Model / Reference: 20384584 FDA UDI
Description: Medical Recording Chart Paper FDA UDI

Identifiers

Catalog Number: 20384584 FDA UDI
Primary DI / UDI-DI: 10884527009633 FDA UDI
FDA Product Code: DSF FDA UDI
GMDN Term: Electrocardiographic recording paper FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 870.2810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 89 Feet FDA UDI
Width — 2 Inch FDA UDI

Category: Electrocardiographic recording paper

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

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Welch Allyn, Inc. — Welch Allyn, Inc. · Class I
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ECG Recording Paper — Diagramma AG · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cardinalhealth

Sources (1)

FDA UDI 80053bf7-aa8a-437a-9207-ca660df0902a 37 fields · synced May 30, 2026