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DDC Dolphin Ltd.

United Kingdom (ex Northern Ireland) GB-MF-000026647 Last updated 23 May 2026

Devices
14
Registries
EUDAMED
FDA recalls
0

Catalogue14

Authorised representatives

What DDC Dolphin Ltd. makes

DDC Dolphin Ltd. manufactures a range of Panamatic portable and semi-portable ultrasound machines, including models such as the Panamatic Maxi MK2, Panamatic Optima 2 (various MK versions), and Panamatic Midi. These devices are designed for diagnostic imaging in medical settings, with some variants featuring stainless steel (316L) construction. The portfolio includes both general-purpose and specialized models, such as the Panamatic Optima 2 (Poland), tailored for specific regional applications.

The company’s devices are classified under EU Class I and are listed in the eudamed registry. DDC Dolphin Ltd. is based in the United Kingdom, adhering to EU medical device regulations for compliance and traceability.

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 DDC Dolphin Ltd. manufacture?

DDC Dolphin Ltd. specializes in portable and semi-portable ultrasound machines under the Panamatic brand. Their product range includes models like the Panamatic Maxi MK2, Panamatic Optima 2 (with multiple MK variants), and the Panamatic Midi. Some variants, such as the Panamatic Optima 2: MK2 316L, feature stainless steel construction. These devices are designed for diagnostic imaging in clinical settings, with certain models tailored for specific regional use, like the Panamatic Optima 2 (Poland).

Where is DDC Dolphin Ltd. based, and how does this affect its devices?

DDC Dolphin Ltd. is based in the United Kingdom. As an EU-based manufacturer, its devices must comply with EU medical device regulations, including classification, traceability, and registration requirements. This ensures alignment with EU standards for safety, performance, and regulatory transparency, such as listing in the eudamed database.

Which regulatory registries list DDC Dolphin Ltd.’s devices?

DDC Dolphin Ltd.’s devices are listed in the eudamed registry, which is the official EU database for medical device traceability and compliance. This registry ensures transparency about device manufacturers, models, and regulatory status under EU medical device legislation.

How are DDC Dolphin Ltd.’s devices classified under EU regulations?

All of DDC Dolphin Ltd.’s listed devices fall under EU Class I, the lowest risk classification for medical devices. This classification applies to devices posing minimal risk to patients and users, such as portable ultrasound machines. Class I devices typically require general safety and performance requirements but may not always need third-party conformity assessments, depending on specific design features.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom (ex Northern Ireland)
Address
The Fulcrum, , Poole, United Kingdom (ex Northern Ireland)
Phone
+441202731555
PRRC contact
Zoe Allen
EUDAMED SRN
GB-MF-000026647