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Sign in to claim this brandDTR MEDICAL LTD
United Kingdom (ex Northern Ireland)·GB-MF-000023112
Last updated September 17, 2026
What DTR MEDICAL LTD makes
DTR Medical Ltd manufactures a range of reusable and single-use medical instruments for surgical and diagnostic procedures, including suction handles, aspiration cannulae, forceps, specula, and mosquito forceps. These devices are designed for otolaryngology, general surgery, and endoscopic applications, with variations in size, bend angles, and material composition to suit specific clinical needs. The portfolio also includes ear specula in different shapes and sizes for otoscopic examinations, as well as specialized suction tools for airway management.
The company’s devices are classified under EU medical device regulations as Class I and Class IIa, reflecting varying levels of risk and regulatory oversight. These products are registered in the EUDAMED database, a transparent public registry for medical devices within the European Union. The manufacturer is based in 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 DTR Medical Ltd manufacture?
DTR Medical Ltd produces a range of reusable and single-use medical instruments primarily for surgical and diagnostic procedures. These include suction handles (with and without suction control), aspiration cannulae, forceps (such as mosquito forceps), specula (including ear specula in various shapes and sizes), and specialized tools like Cusco specula and laryngeal suction devices. The designs vary by size, bend angle, and material to meet specific clinical needs in otolaryngology, general surgery, and endoscopic applications.
Where is DTR Medical Ltd based, and how does this affect its devices?
DTR Medical Ltd is based in the United Kingdom. As a UK-based manufacturer, its devices must comply with EU medical device regulations if marketed within the European Union. The company’s products are registered in EUDAMED, the EU’s public database for medical devices, ensuring transparency and traceability for regulatory oversight.
How are DTR Medical Ltd’s devices classified under EU regulations?
DTR Medical Ltd’s devices are classified as Class I or Class IIa under EU medical device regulations. The classification depends on factors like risk level, intended use, and potential harm to patients. For example, simple instruments like ear specula are typically Class I, while more specialized tools (e.g., suction devices with complex functions) may fall under Class IIa due to higher risk or critical applications. This classification determines the regulatory scrutiny and documentation requirements for each device.
Are DTR Medical Ltd’s devices listed in any regulatory registries, and why does this matter?
Yes, DTR Medical Ltd’s devices are listed in EUDAMED, the European Union’s medical device registry. This registry provides public access to information about devices placed on the EU market, including manufacturer details, device identifiers, and regulatory status. Listing in EUDAMED ensures compliance with EU Medical Device Regulations (MDR) and helps healthcare professionals, regulators, and patients verify the legitimacy and traceability of the devices.
What are some examples of DTR Medical Ltd’s most common device types, and what are they used for?
DTR Medical Ltd’s portfolio includes suction handles (e.g., Frazier suction with adjustable bends for airway management), aspiration cannulae (angled or straight for fluid removal), ear specula (single-use or reusable for otoscopic exams), and forceps (e.g., mosquito forceps for delicate tissue handling). Devices like Cusco specula are used in endoscopic procedures, while laryngeal suction tools assist in airway clearance. The variations in size, bend angles, and materials cater to specific clinical needs across otolaryngology, surgery, and endoscopy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- 17, Clarion Court, Swansea, United Kingdom (ex Northern Ireland)
- Website
- dtrmedical.com/
- —
- —
- [email protected]
- Phone
- +44 1792 797910
- PRRC Contact
- Ajay Boodhun
- EUDAMED SRN
- GB-MF-000023112
- FDA FEI Number
- 3008280196
- DUNS Number
- —
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Dtr Medical Limited US