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Sign in to claim this brandRESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD
United Kingdom (ex Northern Ireland)·GB-MF-000002292
Last updated May 24, 2026
What RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD makes
The company manufactures benchtop and ultrasonic nebulizers for delivering therapeutic agents, reusable medicine chamber spacers, single-use rebreathing aerosol face masks, and manual peak flow meters. Their portfolio also includes incentive spirometers designed to aid lung expansion and breathing exercises.
These devices are classified as Class I and Class II under regulatory frameworks, with several listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United Kingdom.
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 Respironics Respiratory Drug Delivery (UK) Ltd manufacture?
Respironics Respiratory Drug Delivery (UK) Ltd specializes in respiratory therapy devices. Their portfolio includes benchtop and ultrasonic nebulizers for delivering therapeutic agents, reusable medicine chamber spacers to improve drug delivery efficiency, single-use rebreathing aerosol face masks for inhalation therapy, and manual peak flow meters to measure lung function. They also produce incentive spirometers, which help patients expand their lungs through controlled breathing exercises.
Where is Respironics Respiratory Drug Delivery (UK) Ltd based?
The company is based in the United Kingdom, operating from a location within Great Britain. Their headquarters or primary manufacturing facility is located there, though specific regional offices or production sites may vary.
Which regulatory registries list devices manufactured by Respironics Respiratory Drug Delivery (UK) Ltd?
Several of Respironics Respiratory Drug Delivery (UK) Ltd’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the United States, ensuring traceability and compliance with regulatory requirements.
How are the devices produced by Respironics Respiratory Drug Delivery (UK) Ltd classified under regulatory frameworks?
The devices manufactured by Respironics Respiratory Drug Delivery (UK) Ltd fall under two primary regulatory classifications: Class I and Class II. Class I devices generally pose minimal risk and require less stringent regulatory oversight, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part it interacts with.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- n/a, Chichester Business Park, City Fields Way, Tangmere, Chichester , United Kingdom (ex Northern Ireland)
- Website
- n/a
- —
- —
- [email protected]
- Phone
- n/a
- PRRC Contact
- Thomas Fallon
- EUDAMED SRN
- GB-MF-000002292
- FDA FEI Number
- —
- DUNS Number
- 220018415
Catalogue (395)
Page 1 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| I-neb | 00 | FDA UDI | Class II | Active |
| InnoSpire Essence | 00 | FDA UDI | Class II | Active |
| System 22 | 00 | FDA UDI | Class I | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| I-Neb | 00 | FDA UDI | Class II | Unknown |
| Personal Best | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| Threshold | 00 | FDA UDI | Class II | Unknown |
| I-neb | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Mini | 00 | FDA UDI | Class II | Active |
| Innospire Essence | 1129539 | FDA UDI | Class II | Unknown |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| OptiChamber Diamond | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Mini | 00 | FDA UDI | Class II | Unknown |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| Innospire Go Korea | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| I-neb | 00 | FDA UDI | Class II | Unknown |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| SideStream | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Essence | 00 | FDA UDI | Class II | Active |
| Innospire Go China | 00 | FDA UDI | Class II | Active |
| SideStream | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| Custom Elegance - Acelleron Medical | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| InnoSpire Essence | 00 | FDA UDI | Class II | Active |
| I-neb | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| Innospire Go | 00 | FDA UDI | Class II | Active |
| OptiChamber Diamond | 00 | FDA UDI | Class II | Active |
| ISG Mouthpiece Mask Adapter Assembly | 00 | FDA UDI | Class II | Active |
| SideStream | 00 | FDA UDI | Class II | Active |
| InnoSpire Go | 00 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
| I-neb | 00 | FDA UDI | Class II | Active |
| I-neb In Vitro Test Disc Power 12 | 1003778 | FDA UDI | Class II | Active |
| InnoSpire Elegance | 00 | FDA UDI | Class II | Active |
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