Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Electrotherapy equipment -… — Class I MDR by Elektronika i…

MD Atlas
Elektronika i Elektromedycyna M.Lewandowski Sp.J.

EUDAMED last updated this device on Apr 9, 2026

Electrotherapy equipment - Electrode

5906660092WDEE98

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Elektronika i Elektromedycyna M.Lewandowski Sp.J.
UDI-DI code: 05906660092711
Reference / catalog number: E-A75N

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

Organization name: Elektronika i Elektromedycyna M.Lewandowski Sp.J.
SRN: PL-MF-000032400
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: Electrotherapy equipment - Electrode
UDI-DI code: 05906660092711
Basic UDI-DI: 5906660092WDEE98
Reference / catalog number: E-A75N
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05906660092711

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

N010201TENS SYSTEM ELECTRODES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas

Related devices

Physiotherapy equipment - trolley5906660092WDFDSOn the market CARBObed5906660092CARB5On the market Electrotherapy equipment - Electrode5906660092WDEE98On the market Electrotherapy equipment - Electrode5906660092WDEE98On the market Electrotherapy equipment - Electrode5906660092WDEE98On the market

Certificates

Certificate health across this manufacturer's portfolio.

TNP/MDR/0030/2034/2025Issued
Quality management systemNotified body: 2274Expiry: Jan 16, 2028