← Back to catalogue

Welch Allyn, Inc.

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 721360Model 901006

by Welch Allyn, Inc.

Identity

Trade Name
ECG Accessory Cardiopulmonary EUDAMED
Welch Allyn, Inc. FDA UDI
Generic Name
Electrocardiographic lead set, reusable FDA UDI
Device Name
10-LEAD PAT CABLE AHA PINCH CP50 150 FDA UDI
Model / Reference
901006 EUDAMEDFDA UDI
721360 EUDAMED
Description
10-LEAD PAT CABLE AHA PINCH CP50 150 FDA UDI

Identifiers

Catalog Number
721360 FDA UDI
Primary DI / UDI-DI
00732094192513 EUDAMEDFDA UDI
Basic UDI-DI
0732094GMN901006FNS EUDAMED
510(k) Number
K972121 FDA UDI
FDA Product Code
MLD FDA UDI
EMDN Code
Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Electrocardiographic lead set, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.1025 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Electrocardiographic lead set, reusable

Welch Allyn, Inc. by Welch Allyn, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Welch Allyn, Inc.

Sources (2)

  • FDA UDI 552636b1-d45b-4b2b-a986-3ed064d11caa 36 fields · synced Jul 29, 2026
  • EUDAMED 1726ecbf-1233-4ff9-baa4-3fc3c74c2970 61 fields · synced Jul 29, 2026