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50x50mm Electrode
EUDAMEDFDA UDIClass I (EU MDR)
Ref E-CM5050Model Adhesive Electrodes
by TensCare Ltd
Identity
- Trade Name
- 50x50mm Electrode EUDAMEDTensCare FDA UDI
- Generic Name
- Transcutaneous electrical stimulation electrode, single-use FDA UDI
- Device Name
- Electrode, transcutaneous, electric nerve EUDAMEDThe Carbon Mesh Electrode pads 50x50 mm, is a pack of 4 reusable electrodes, with an intended use for the desired success of any stimulation (TENS or EMS). They are intended for a single user. FDA UDI
- Model / Reference
- Adhesive Electrodes EUDAMEDE-CM5050 EUDAMEDCarbon Mesh Electrode pads 50x50 mm FDA UDI
- Description
- The Carbon Mesh Electrode pads 50x50 mm, is a pack of 4 reusable electrodes, with an intended use for the desired success of any stimulation (TENS or EMS). They are intended for a single user. FDA UDI
Identifiers
- Catalog Number
- E00013 FDA UDI
- Primary DI / UDI-DI
- 05033435000500 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 EUDAMEDClass 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
50x50mm 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 5033435E00013WR | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- TensCare Ltd
- EUDAMED SRN
- GB-MF-000004156
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 961080ac-2962-4844-b3e2-7e63ca1d0673 61 fields · synced Jul 31, 2026
- FDA UDI 8bbe9b11-c07e-4bfc-abe2-b1a3a7ac2793 35 fields · synced May 30, 2026