← Back to catalogue

Es-5200

EUDAMED

Class IIa (EU MDR)

Ref ES-5200

by Ito Co., Ltd.

Identity

Trade Name
ES-5200 EUDAMED
Device Name
ES-5200 EUDAMED
Model / Reference
ES-5200 EUDAMED

Identifiers

Primary DI / UDI-DI
04983087011410 EUDAMED
Basic UDI-DI
B-04983087011410 EUDAMED
EMDN Code
Z120601 ELECTROTHERAPY EQUIPMENT (INCLUDED TENS) EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Es-5200 by Ito Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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

Manufacturer

Manufacturer
Ito Co., Ltd.
EUDAMED SRN
JP-MF-000021681
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 0f14e346-1038-47ba-acda-e95655b3c6e8 61 fields · synced Jun 19, 2026