DDC Dolphin Ltd.
GB-MF-000026647 · United Kingdom · Poole
DDC Dolphin Ltd. is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Most frequent device types declared: Panamatic Range.
Authorised representative in the Union: Advena SRL.
Devices declared under this manufacturer
- Panamatic Maxi MK1
- Panamatic Maxi MK2
- Panamatic Midi
- Panamatic Midi MK2
- Panamatic Optima 1 POL-MK2
- Panamatic Optima 2
- Panamatic Optima 2 (Poland)
- Panamatic Optima 2 MK1
- Panamatic Optima 2: MK2
- Panamatic Optima 2: MK2 316L
- Panamatic Optima 3 MK1
- Panamatic Optima 3 MK2
Showing 12 of 14 declared devices.
Catalogue references include 17-17-0000-E, 17-17-0000-E-MK2, 17-17-0000-ITA-MK2, 17-17-0090-E, 17-17-0090-E-MK2, 17-17-0090-ITA-MK2.
European nomenclature codes declared: V0799.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 14 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. DDC Dolphin Ltd. was not found in either the U.S. or the Canadian register.