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Wireless Patient Module

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref CIE-01B

by Fukuda Denshi Co., Ltd.

Identity

Trade Name
Wireless Patient Module EUDAMED
FUKUDA DENSHI FDA UDI
Generic Name
Patient monitoring system module, electrocardiographic, telemetric FDA UDI
Device Name
Electrocardiograph EUDAMED
Model / Reference
CIE-01B EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04538612915987 EUDAMED
04538612915994 FDA UDI
Basic UDI-DI
4538612010009E EUDAMED
510(k) Number
K173226 FDA UDI
FDA Product Code
DPS FDA UDI
EMDN Code
Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Patient monitoring system module, electrocardiographic, telemetric FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.2340 FDA UDI
Market of Registration
Germany 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic lead set, reusable

Wireless Patient Module by Fukuda Denshi Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
JP-MF-000008253
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED fd918483-9ee9-4361-ae01-202dcc5bcd4a 61 fields · synced Jul 14, 2026
  • FDA UDI 6ec5b5cc-3516-4c6c-970a-5ce66be6ba5b 33 fields · synced May 29, 2026