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Welch Allyn, Inc.

FDA UDI

Class I (US FDA UDI)

by Welch Allyn, Inc.

Identity

Trade Name
Welch Allyn, Inc. FDA UDI
Generic Name
Electrocardiographic recording paper FDA UDI
Device Name
Assurance Paper, cued with header A4. For use with EL 250 and 250c, ELI 280, and ELI 350. 250 sheets/pack, 12 packs/case. Price per case. FDA UDI
Model / Reference
901136 FDA UDI
Description
Assurance Paper, cued with header A4. For use with EL 250 and 250c, ELI 280, and ELI 350. 250 sheets/pack, 12 packs/case. Price per case. FDA UDI

Identifiers

Catalog Number
9100-026-54 FDA UDI
Primary DI / UDI-DI
20817655021175 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic recording paper

Welch Allyn, Inc. by Welch Allyn, 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

Manufacturer
Welch Allyn, Inc.

Sources (1)

  • FDA UDI 8d538d44-c24a-4106-bc3a-e3d3e0221d35 35 fields · synced Jun 1, 2026