Exmoor Plastics Limited
GB-MF-000025513 · United Kingdom · Chorley
Exmoor Plastics Limited is registered in the European database on medical devices as a manufacturer, with 131 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 32 |
|---|---|
| Class IIa | 99 |
Most frequent device types declared: AS8, E101, E108x5, E110x5, E116.
Among these devices, 131 are declared sterile, 32 implantable.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Aural Speculum Oval/Bevelled, Set of 3 (ASS, AS6, AS7)
- Brown Nasal Splint\tL 68 mm x W 23 mm x Thickness 0.85 mm
- Collar Button 1.14 mm
- Grimaldi Nasal Splint L64 mm x W 30 mm x Thickness 0.85 mm
- Myringotomy Kit with Grasper Forceps and Curved Needle
- Plain Sucker Fine End
- Reuter Bobbin 1.14 mm
- Shah Mini Tube 0.85mm
- Shah Vent Tube without wire 1.14 mm
- Shepards Drain with wire 0.97 mm
- Shepards Drain with wire 1.4mm
- Shepards Drain without wire 0.97 mm
Showing 12 of 131 declared devices.
Catalogue references include AS8, E101, E108x5, N3, N5, UK3-175SF.
European nomenclature codes declared: Q030399, Q03040101, Q0399, Q030316, Q030301.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Exmoor Plastics Limited (GB) · FDA 3002806953 |
| Devices in EUDAMED | 131 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 131 |
|---|---|
| Found in the U.S. device database | 130 |
| Share | 99.2 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | EXMOOR PLASTICS |
North American profile: Both markets. Exmoor Plastics Limited is registered in both the United States and Canada.