LM Global Design Limited
IE-MF-000046744 · Ireland · Dublin
LM Global Design Limited is registered in the European database on medical devices as a manufacturer, with 363 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 363 |
|---|
Most frequent device types declared: AQUATEC PURE CALA.
Devices declared under this manufacturer
- ARMRESTS FOR SS1/SC1/CMD RANGE BLACK KD
- ARMRESTS FOR SS1/SC1/CMD RANGE WHITE KD
- BACKREST FOR BATHTUB SEAT KING
- BACKREST FOR SS1/SC1/CMD RANGE
- FOLDING BAR 60 CM STAINLESS STEEL POLISHED KING
- FOLDING BAR 60 CM/24IN POWDER COATED WHITE KD
- RAISED TOILET SEAT NIVELLA 150
- RTS 12 CM/5IN KING
- RTS 12 CM/5IN W/FIXED ARMRESTS FARMACARE KD
- RTS 15 CM/6IN W/LID SANIPLAST KD
- SHOWER CHAIR W/BACKREST BLACK KING
- SHOWER SEAT WHITE KD
Showing 12 of 363 declared devices.
Catalogue references include AR-14-PP-18, EH-BA-PP-BX, EH-BSTA-PP-BX, EH-NWA-60-PCX, EH-SSA-PP-B, KING-15-33.
European nomenclature codes declared: Y093303, Y091215, Y181803, Y090699, Y091203, Y091299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LM GLOBAL DESIGN LIMITED (IE) · FDA 3011310591 |
| Devices in EUDAMED | 363 |
| Country of registration | Ireland |
Device-level evidence
| Devices with a numeric GTIN | 363 |
|---|---|
| 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: United States only. LM Global Design Limited is registered in the United States but was not found in the Canadian register.