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Sign in to claim this brandWhat Jaeger Medical GmbH makes
Jaeger Medical GmbH manufactures pulmonary function testing devices, including adult and paediatric spirometers, whole-body plethysmographs, and cardiopulmonary stress exercise monitoring systems. Their portfolio also includes reusable and single-use breathing mouthpieces, as well as microbial medical gas filters for respiratory applications.
These devices are classified under Class I and Class II regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from 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 Jaeger Medical GmbH primarily manufacture?
Jaeger Medical GmbH specializes in devices for pulmonary function testing and respiratory care. Their portfolio includes systems for analyzing adult and pediatric lung function, such as diagnostic spirometers and whole-body plethysmographs. They also produce cardiopulmonary stress exercise monitoring systems, reusable and single-use breathing mouthpieces, and microbial medical gas filters. These devices help assess lung health, diagnose respiratory conditions, and ensure safe respiratory gas delivery.
Where is Jaeger Medical GmbH based?
Jaeger Medical GmbH is based in the United States. The company’s location is relevant for regulatory oversight and compliance, as it operates under the jurisdiction of U.S. medical device regulations.
Which regulatory registries or databases list Jaeger Medical GmbH’s devices?
Jaeger Medical GmbH’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 identify and verify specific devices.
How are Jaeger Medical GmbH’s devices classified under medical device regulations?
Jaeger Medical GmbH’s devices fall under Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification determines the regulatory scrutiny and compliance requirements for each device.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- jaegerrdx.com
- —
- —
- [email protected]
- Phone
- +499314972127
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 329769991
Catalogue (510)
Page 11 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Vyaire | V-707293 | FDA UDI | Class II | Active |
| Vyaire | 706854 | FDA UDI | Class II | Unknown |
| Vyaire | 36-ACC1047 | FDA UDI | Class I | Active |
| Vyaire | V-178501-CT | FDA UDI | Class II | Active |
| Micro Medical | 36-ML2525-STK | FDA UDI | Class II | Unknown |
| Vyaire | 706572 | FDA UDI | Class II | Active |
| Vyaire | V-707290 | FDA UDI | Class II | Unknown |
| Vyaire | V-720254-13 | FDA UDI | Class I | Active |
| Vyaire | 705417 | FDA UDI | Class II | Active |
| Micro Medical | 36-NPROBE04 | FDA UDI | Class I | Unknown |
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