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Sign in to claim this brandWhat Savaria Concord Lifts Inc makes
Savaria Concord Lifts Inc manufactures overhead track systems for patient lifting and transfers, electrically-powered mobile patient lifts, and assistive passenger lifts. Their product line also includes stairlifts designed for chair use and turntable mechanisms for patient repositioning.
The company’s devices are classified under FDA’s Class I and Class II categories 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 Savaria Concord Lifts Inc manufacture?
Savaria Concord Lifts Inc specializes in devices designed to assist with patient mobility and transfers. Their product line includes overhead track systems for lifting and transferring patients, electrically-powered mobile patient lifts, and assistive passenger lifts. They also produce stairlifts for chair use and turntable mechanisms to help reposition patients. These devices are engineered to support healthcare settings where safe and efficient patient handling is critical.
Where is Savaria Concord Lifts Inc 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 in the U.S. market.
Which regulatory registries or databases list Savaria Concord Lifts Inc’s devices?
Savaria Concord Lifts Inc’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, ensuring they can identify and verify the devices in use. The UDI system is a key component of the FDA’s efforts to improve patient safety and device tracking.
How are Savaria Concord Lifts Inc’s devices classified under FDA regulations?
The company’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose the lowest risk and are subject to general controls, while Class II devices require additional performance standards to ensure their safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with, as outlined in FDA guidelines.
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
- 245449095
Catalogue (144)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| M-Series | M2F272-1202-02-NA | FDA UDI | Class I | Active |
| M-Series | M4F200-1200-02-NA | FDA UDI | Class I | Active |
| Monarch | M921250 | FDA UDI | Class I | Active |
| Monarch | M929301 | FDA UDI | Class I | Active |
| Monarch | M929331 | FDA UDI | Class I | Active |
| Monarch | M929211-05 | FDA UDI | Class I | Active |
| Monarch | M929111-05 | FDA UDI | Class I | Active |
| Monarch | M929231 | FDA UDI | Class I | Active |
| M-Series | M2F200-1200-00-NA | FDA UDI | Class I | Active |
| M-Series | M4F272-1100-00-NA | FDA UDI | Class I | Active |
| Monarch | M921275 | FDA UDI | Class I | Active |
| M-Series | M4F200-1200-00-NA | FDA UDI | Class I | Active |
| Monarch | M929341-07 | FDA UDI | Class I | Active |
| Monarch | M929011 | FDA UDI | Class I | Active |
| M-Series | M2F272-1202-00-NA | FDA UDI | Class I | Active |
| M-Series | M2F272-1102-08-NA | FDA UDI | Class I | Active |
| M-Series | M4F200-1203-02-NA | FDA UDI | Class I | Active |
| Monarch | M929251 | FDA UDI | Class I | Active |
| Monarch | M929221-04 | FDA UDI | Class I | Active |
| M-Series | M2F272-1102-02-NA | FDA UDI | Class I | Active |
| Monarch | M929221-01 | FDA UDI | Class I | Active |
| M-Series | M2F272-1100-00-NA | FDA UDI | Class I | Active |
| M-Series | M4F200-1100-02-NA | FDA UDI | Class I | Active |
| Monarch | M929001 | FDA UDI | Class I | Active |
| Monarch | M929131 | FDA UDI | Class I | Active |
| Monarch | M929121-06 | FDA UDI | Class I | Active |
| Monarch | M929221-02 | FDA UDI | Class I | Active |
| M-Series | MBA454-1113-00-NA | FDA UDI | Class I | Active |
| Turntable | M929513 | FDA UDI | Class I | Active |
| M-Series | M2F200-1100-06-NA | FDA UDI | Class I | Active |
| M-Series | M2F200-1102-02-NA | FDA UDI | Class I | Active |
| Monarch | M929401 | FDA UDI | Class I | Active |
| M-Series | M2F200-1100-08-NA | FDA UDI | Class I | Active |
| Monarch | M929211 | FDA UDI | Class I | Active |
| Monarch | M929221-05 | FDA UDI | Class I | Active |
| M-Series | M4F272-1400-00-NA | FDA UDI | Class I | Active |
| M-Series | M2F272-1100-06-NA | FDA UDI | Class I | Active |
| Turntable | M929514 | FDA UDI | Class I | Active |
| Monarch | M929221 | FDA UDI | Class I | Active |
| M-Series | M2F200-1102-08-NA | FDA UDI | Class I | Active |
| Monarch | M929201-10 | FDA UDI | Class I | Active |
| M-Series | M2F272-1203-02-NA | FDA UDI | Class I | Active |
| M-Series | M4F200-1100-00-NA | FDA UDI | Class I | Active |
| Savaria | V1504D | FDA UDI | Class II | Active |
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