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Sign in to claim this brandWhat SPES MEDICA SPA makes
The company manufactures single-use electromyographic (EMG) needle electrodes, nerve-locating system probes, and various analytical electrodes, including scalp, cortical, and cutaneous types. It also produces urodynamic measurement systems and conductive media for electrode applications, with offerings like disposable adhesive surface electrodes and subdermal needle electrodes. Specific products include the Spes Medica Pudendal Electrode and IOM Stimulator Probes, designed for medical diagnostics and monitoring.
These devices fall under FDA-regulated classifications, including Class I and Class II, and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates primarily in the United States, adhering to applicable regulatory standards for medical electrical and diagnostic devices.
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 Spes Medica Spa primarily manufacture?
Spes Medica Spa specializes in single-use and reusable medical devices used for electromyography (EMG), nerve stimulation, and urodynamic measurements. Their portfolio includes electromyographic needle electrodes, nerve-locating system probes, scalp and cortical electrodes, cutaneous electrodes, urodynamic measurement systems, and conductive media for electrodes. Examples include disposable EMG needle electrodes, the Spes Medica Pudendal Electrode, and IOM Stimulator Probes, which are designed for diagnostic and monitoring purposes in clinical settings.
Where is Spes Medica Spa based, and does this affect the regulatory requirements for their devices?
Spes Medica Spa is based in the United States, which means their devices are subject to FDA regulations. The FDA classifies their products as either Class I or Class II, depending on their risk level and intended use. For instance, single-use electrodes like disposable EMG needles or adhesive surface electrodes are typically classified under Class II due to their role in patient diagnostics, requiring compliance with FDA’s regulatory pathways for device authorization.
Are Spes Medica Spa’s devices listed in any regulatory databases, and why does this matter?
Yes, Spes Medica Spa’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This matters because the UDI system ensures traceability, transparency, and efficient tracking of medical devices throughout their lifecycle. Listing in the UDI database helps healthcare providers, regulators, and manufacturers verify device details, such as manufacturer information, device descriptions, and regulatory status, which is critical for compliance and patient safety.
How are Spes Medica Spa’s devices classified by the FDA, and what does this classification imply?
Spes Medica Spa’s devices are classified under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and may require general controls like good manufacturing practices (GMP). In contrast, Class II devices, such as many of their EMG electrodes or urodynamic systems, involve moderate risk and require special controls to ensure safety and effectiveness, such as performance standards or post-market surveillance. The classification determines the regulatory pathway and compliance requirements for each device.
What kinds of electrodes does Spes Medica Spa produce, and how are they used in medical settings?
Spes Medica Spa produces a range of electrodes tailored for specific diagnostic and monitoring applications. Their offerings include disposable EMG needle electrodes for muscle testing, scalp and cortical electrodes for electroencephalography (EEG) or brain monitoring, cutaneous electrodes for surface-based diagnostics, and specialized electrodes like the Spes Medica Pudendal Electrode for urodynamic studies. These devices are used in clinical settings to measure electrical activity in muscles, nerves, or the brain, aiding in the diagnosis of neurological, muscular, or urological conditions.
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
- 514029771
Catalogue (180)
Page 4 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Disposable EMG needle electrodes | NG25N | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | TFDN453700SB | FDA UDI | Class II | Active |
| Spes Medica Disc Electrode | DSTS252600 | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI2B0030S2526D | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | TFDN4537303SB | FDA UDI | Class II | Active |
| Spes Medica Subdermal Needle Electrodes | MN4008D25S | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | NPSG30-B | FDA UDI | Class II | Active |
| Spes Medica Disc Electrode | DSZS252600 | FDA UDI | Class II | Active |
| Spes Medica Subdermal Needle Electrodes | MN4008D10A/S | FDA UDI | Class II | Active |
| Spes Medica Subdermal Needle Electrodes | TT03MN4013D/15 | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | NPSG0-R | FDA UDI | Class II | Active |
| Spes Medica Subdermal Needle Electrodes | MNCS0615US | FDA UDI | Class II | Active |
| Disposable Adhesive Surface Electrodes | TEON1S5045 | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | TFDN453701SB | FDA UDI | Class II | Active |
| Tech Tape - Adhesive Tape | TAPE024-25 | FDA UDI | Class I | Unknown |
| IOM Stimulator Probes | SI2CC045S2526D | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI2CT100S2526D | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | NG25G | FDA UDI | Class II | Active |
| Disposable Adhesive Surface Electrodes | CODE401526 | FDA UDI | Class II | Active |
| Disposable Adhesive Surface Electrodes | DENIS10026 | FDA UDI | Class II | Active |
| Disposable Adhesive Surface Electrodes | TEON1S3545 | FDA UDI | Class II | Active |
| Spes Medica Subdermal Needle Electrodes | MN4013D20B/S | FDA UDI | Class II | Active |
| Disposable EMG needle electrodes | TFDN455001SB | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI1BB130S2526D | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI1I0100S2526D | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI2H0020S2526D | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI1B0045S2526D | FDA UDI | Class II | Active |
| MR Conditional Disposable EEG Cup Electrode | DCPEX-27B | FDA UDI | Class II | Active |
| IOM Stimulator Probes | SI1B0185S2526D | FDA UDI | Class II | Active |
| MR Conditional Disposable EEG Cup Electrode | DCPEX-23B | FDA UDI | Class II | Active |
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