DTR MEDICAL LTD
GB-MF-000023112 · United Kingdom · Swansea
DTR MEDICAL LTD is registered in the European database on medical devices as a manufacturer, with 162 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 162 |
|---|
Most frequent device types declared: Cervical Biopsy Punch, Forceps, Gynaecological Instruments, Non Sterile Ear Specula, Non Sterile Silicone Tubing.
Among these devices, 123 are declared sterile.
Authorised representative in the Union: Emergo Europe B.V..
Devices declared under this manufacturer
- Cervical Biopsy Punch
- Crile Artery Forceps, 140mm Curved on Flat
- Crocodile Fine Jaw Micro Forceps, black finish
- Crocodile Micro Forceps, black finish
- DeBakey Atraumatic Dissecting Forceps 160mm
- Fine Suture Forceps, Plain 105mm
- Fine Suture Forceps, Serrated 105mm
- Frazier Lampert type, 2mm x 125mm, proximal bend with suction control
- Frazier Suction Handle 204 x 2.66mm OD (8Fg), straight, Cross fenestra
- Frazier Suction Handle 204 x 4mm OD (12Fg)
- Kocher-Ochsner 1x2 Toothed Forceps Straight 185mm
- Mosquito Forceps Curved 125mm
Showing 12 of 162 declared devices.
Catalogue references include CFB2001-S, CFBF2001-S, FSF2048, FSH2012, KOF2181, MQC2025-D.
European nomenclature codes declared: A06010103, V9012, Q030499, U089006, A0601010299, Q030304.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DTR MEDICAL LTD (GB) · FDA 3008280196 |
| Devices in EUDAMED | 162 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 162 |
|---|---|
| Found in the U.S. device database | 76 |
| Share | 46.9 % |
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: United States only. DTR MEDICAL LTD is registered in the United States but was not found in the Canadian register.