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100mm x 22m ECG Printer Paper (2/roll)

FDA UDI

Class I (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
100mm x 22m ECG Printer Paper (2/roll) FDA UDI
Generic Name
Electrocardiographic recording paper FDA UDI
Device Name
PAPER ROLLS, 100MM WIDE,ECG FDA UDI
Model / Reference
11240 FDA UDI
Description
PAPER ROLLS, 100MM WIDE,ECG FDA UDI

Identifiers

Catalog Number
11240-000016 FDA UDI
Primary DI / UDI-DI
00883873806296 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic recording paper

100mm x 22m ECG Printer Paper (2/roll) by PHYSIO-CONTROL, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic recording paper.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de0b5eb7-62bd-477f-8421-49ce0f2921dc 35 fields · synced Jun 9, 2026