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H3+ Patient Cable

EUDAMED

Class I (EU MDR)

Ref 9293-037-50Model 901006

by Welch Allyn, Inc.

Identity

Trade Name
H3+ Patient Cable EUDAMED
Model / Reference
901006 EUDAMED
9293-037-50 EUDAMED

Identifiers

Primary DI / UDI-DI
00732094356311 EUDAMED
Basic UDI-DI
0732094GMN901006DNN EUDAMED
EMDN Code
Z12050480 HOLTER SYSTEM INSTRUMENTS FOR CARDIOVASCULAR PARAMETERS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Electrocardiographic lead set, reusable

H3+ Patient Cable by Welch Allyn, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Welch Allyn, Inc.
EUDAMED SRN
US-MF-000013394
Authorised Representative
Welch Allyn Limited IE-AR-000000768

Sources (1)

  • EUDAMED ea25dd7a-091b-46ce-adf3-fc1e64774d8e 61 fields · synced Jul 12, 2026