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Joint Electrode

EUDAMEDFDA UDI

Class I (EU MDR)

Ref E-CMSF150Model Adhesive Electrodes

by TensCare Ltd

Identity

Trade Name
Joint Electrode EUDAMED
TensCare FDA UDI
Generic Name
Transcutaneous electrical stimulation electrode, single-use FDA UDI
Device Name
Electrode, transcutaneous, electric nerve EUDAMED
The Joint Electrode pad, is a pack of 1 reusable electrode designed for joints, with an intended use for the desired success of any stimulation (TENS or EMS). it is intended for a single user. FDA UDI
Model / Reference
Adhesive Electrodes EUDAMED
E-CMSF150 EUDAMED
Joint Electrode pad FDA UDI
Description
The Joint Electrode pad, is a pack of 1 reusable electrode designed for joints, with an intended use for the desired success of any stimulation (TENS or EMS). it is intended for a single user. FDA UDI

Identifiers

Catalog Number
E00019 FDA UDI
Primary DI / UDI-DI
05033435133147 EUDAMEDFDA UDI
Basic UDI-DI
5033435E00013WR EUDAMED
510(k) Number
K210448 FDA UDI
FDA Product Code
GXY FDA UDI
EMDN Code
N010201 TENS SYSTEM ELECTRODES EUDAMED
GMDN Term
Transcutaneous electrical stimulation electrode, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.1320 FDA UDI
Market of Registration
Poland 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Joint Electrode by TensCare Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
TensCare Ltd
EUDAMED SRN
GB-MF-000004156
Authorised Representative
Advena Limited MT-AR-000000234

Sources (2)

  • EUDAMED 72179fd9-c10a-414e-bf95-272885366c69 61 fields · synced Jun 19, 2026
  • FDA UDI 347c4c7e-8a6f-4a6c-b7e6-3bd314ddddb1 35 fields · synced May 29, 2026