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US
Last updated May 30, 2026
Part of Nissha Medical Technologies Ltd
What NISSHA MEDICAL TECHNOLOGIES SAS makes
The company manufactures single-use electrosurgical return electrodes, reusable electrocardiographic lead sets and electrodes, single-use surgical irrigation tubing sets, and reusable electrical-only medical device connection cables.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 NISSHA MEDICAL TECHNOLOGIES SAS manufacture?
NISSHA MEDICAL TECHNOLOGIES SAS produces a range of medical devices, including single-use electrosurgical return electrodes (like the Swaroplate), reusable electrocardiographic lead sets and electrodes (such as those in the INTEGRAL PROCESS Cables & Leadwires series), single-use surgical irrigation tubing sets, and reusable electrical-only medical device connection cables. These devices are designed for use in surgical and diagnostic procedures.
Where is NISSHA MEDICAL TECHNOLOGIES SAS based?
NISSHA MEDICAL TECHNOLOGIES SAS is based in the United States. The company’s location is relevant for understanding its regulatory scope and compliance framework, particularly under FDA guidelines.
Which regulatory registries list NISSHA MEDICAL TECHNOLOGIES SAS’s devices?
NISSHA MEDICAL TECHNOLOGIES SAS’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to verify device details and compliance.
How are NISSHA MEDICAL TECHNOLOGIES SAS’s devices classified under FDA regulations?
All of NISSHA MEDICAL TECHNOLOGIES SAS’s devices fall under Class II classification according to FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls beyond general 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
- —
- Website
- nisshamedical.com
- —
- —
- [email protected]
- Phone
- +33139726666
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 391906658
Catalogue (152)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Swaroplate | 1222H | FDA UDI | Class II | Active |
| Vermed | F7952W | FDA UDI | Class II | Unknown |
| ELUXEO Tubing | 35831400 | FDA UDI | Class II | Active |
| Vermed | F7967 | FDA UDI | Class II | Unknown |
| INTEGRAL PROCESS Cables & Leadwires | 72466-US | FDA UDI | Class II | Active |
| Vermed | F7950W | FDA UDI | Class II | Unknown |
| INTEGRAL PROCESS Cables & Leadwires | 70612SJ5-US | FDA UDI | Class II | Active |
| INTEGRAL PROCESS Cables & Leadwires | 72712-US | FDA UDI | Class II | Active |
| Vermed | F7950PL | FDA UDI | Class II | Unknown |
| Vermed | F7958 | FDA UDI | Class II | Unknown |
| Vermed | F7952W/1 | FDA UDI | Class II | Unknown |
| Swaroplate | 1269H | FDA UDI | Class II | Active |
| Boston Scientific | DGP-PM2-25 | FDA UDI | Class II | Active |
| Vermed | F7961 | FDA UDI | Class II | Unknown |
| Vermed | F7953P | FDA UDI | Class II | Unknown |
| Claravue | CLARAVUE PM M5 RT US | FDA UDI | Class II | Active |
| Maestro | 1291H | FDA UDI | Class II | Active |
| ELUXEO Tubing Kit | 35841703 | FDA UDI | Class II | Active |
| INTEGRAL PROCESS Cables & Leadwires | 70611NGJ3-US | FDA UDI | Class II | Active |
| Vermed | F7951W/1 | FDA UDI | Class II | Unknown |
| INTEGRAL PROCESS Cables & Leadwires | 72350-US-5.5M | FDA UDI | Class II | Active |
| ELUXEO Tubing | 35831300 | FDA UDI | Class II | Active |
| ELUXEO Hybrid Tubing | 35811672 | FDA UDI | Class II | Active |
| Claravue | CLARAVUE PM 12 RT CARDIO | FDA UDI | Class II | Active |
| Vermed | F7752 | FDA UDI | Class II | Unknown |
| Stryker | 0406-650-205 | FDA UDI | Class II | Active |
| INTEGRAL PROCESS Cables & Leadwires | ECG Cable | FDA UDI | Class II | Active |
| Vermed | 70646NGJ10 | FDA UDI | Class II | Active |
| Vermed | F7956W | FDA UDI | Class II | Unknown |
| Swaroplate | 1213H | FDA UDI | Class II | Active |
| Vermed | 72350-US | FDA UDI | Class II | Active |
| Swaroplate | 1263H | FDA UDI | Class II | Active |
| Swaroplate | 1220H | FDA UDI | Class II | Active |
| INTEGRAL PROCESS Cables & Leadwires | ECG Cable | FDA UDI | Class II | Active |
| Vermed | F7957PL | FDA UDI | Class II | Unknown |
| Swaroplate | 1261H | FDA UDI | Class II | Active |
| Vermed | F7954 | FDA UDI | Class II | Unknown |
| Vermed | F7951W | FDA UDI | Class II | Unknown |
| Swaroplate | 1286H | FDA UDI | Class II | Active |
| Vermed | F7955 | FDA UDI | Class II | Unknown |
| Swaroplate | 1257H | FDA UDI | Class II | Active |
| Vermed | F7966W | FDA UDI | Class II | Unknown |
| Vermed | F7981P | FDA UDI | Class II | Unknown |
| Vermed | F7956P | FDA UDI | Class II | Unknown |
| Vermed | F7960W | FDA UDI | Class II | Unknown |
| Swaroplate | 1258H | FDA UDI | Class II | Active |
| Swaroplate | 1226H | FDA UDI | Class II | Active |
| Vermed | F7967P | FDA UDI | Class II | Unknown |
| Swaroplate | 1262H | FDA UDI | Class II | Active |
| Swaroplate | 1288H | FDA UDI | Class II | Active |
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