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Sign in to claim this brandMEDICO ELECTRODES INTERNATIONAL LIMITED
US
Last updated May 24, 2026
What MEDICO ELECTRODES INTERNATIONAL LIMITED makes
Medico Electrodes International Limited manufactures single-use electrocardiographic electrodes, designed for temporary attachment to the skin to monitor heart activity. They also produce electrode skin abrasion pads, which prepare the skin to improve electrode adhesion and signal quality during cardiac monitoring procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Medico Electrodes International Limited manufacture?
Medico Electrodes International Limited specializes in single-use electrocardiographic electrodes, which are designed for temporary attachment to the skin to monitor heart activity. They also produce electrode skin abrasion pads, which help prepare the skin to ensure better electrode adhesion and signal clarity during cardiac monitoring. These devices are primarily used in clinical settings for accurate and reliable heart rhythm assessment.
Where is Medico Electrodes International Limited based?
The company is headquartered in the United States. This location allows them to operate within the regulatory framework of the FDA, which governs the classification and listing of their medical devices.
Which regulatory registries list Medico Electrodes International Limited’s devices?
Medico Electrodes International Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their Class II electrocardiographic electrodes and skin abrasion pads, ensuring transparency and traceability in the medical device supply chain.
How are Medico Electrodes International Limited’s devices classified under FDA regulations?
The company’s devices, including electrocardiographic electrodes and skin abrasion pads, are classified as Class II medical devices by the FDA. This classification is based on their intended use—where they pose moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 677425215
Catalogue (52)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ambu WhiteSensor | 0715M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4242-00-S/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 2121M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/RT/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/L5/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 5050-00-S/10 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/30 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4831Q | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/10 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 7841P/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/3 | FDA UDI | Class II | Active |
| Ambu BlueSensor | BS-TAB-2300/100 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 3245D/RT/60 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WSP30-00-S/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 7841P | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/RT/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4440/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WSP30-00-S/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | CMM/1-00-S/30 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4535M/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 0315M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4535M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 0415M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4570M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4841P | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 5050-00-S/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4242-00-S/10 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WSP25-00-S/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/4 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 5050-00-S/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4500M-H/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 7841P/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4242-00-S/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4500M/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4500M-H/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4440/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4535M/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4242-00-S/50 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 5050-00-S/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WSP30-00-S/5 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4560M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4200 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4500M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4500M-H | FDA UDI | Class II | Active |
| Ambu WhiteSensor | WS-00-S/RT/3 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 0615M | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 4440 | FDA UDI | Class II | Active |
| Ambu WhiteSensor | 0215M | FDA UDI | Class II | Active |
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