MEDI CARE SYSTEM SLU
US Last updated 24 May 2026
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- Devices
- 134
- Registries
- EUDAMEDGUDIDFDA
- FDA recalls
- 0
Catalogue
Salvaclip SCP4100L Ref SCP4100L
Salvafix Transit SVF3476 Ref SVF3476
Salvaclip Comfort SCC4106 Ref SCC4106
Mobi-tools translide TTE6102 Ref TTE6102
Salvaclip SCP4200L Ref SCP4200L
Salvaclip Safe SCF4155 Ref SCF4155
Salvaclip SCP4300 Ref SCP4300
Salvaclip SCP4300L Ref SCP4300L
Salvaclip Comfort SCC4416 Ref SCC4416
Salvaclip Safe SCF4266 Ref SCF4266
Mobi-tools Slide TMS6325 Ref TMS6325
Salvafix Transit SVF3276 Ref SVF3276
Mobi-tools Slide TMS6370 Ref TMS6370
Salvaclip Comfort SCC4415 Ref SCC4415
Mobi-tools Grip TMT6505 Ref TMT6505
Mobi-tools Grip TMT6540 Ref TMT6540
Salvacel SVC2350 Ref SVC2350
Mobi-tools Slide TMS6360 Ref TMS6360
Salvaclip Comfort SCC4406 Ref SCC4406
Mobi-tools translide TTE6108 Ref TTE6108
Mobi-tools Turn TMT6550 Ref TMT6550
Medi-Roller Pro TMR6275 Ref TMR6275
Salvaclip Safe SCF4365 Ref SCF4365
Salvacel SVC2510 Ref SVC2510
Medi-Glide TMG6430 Ref TMG6430
Salvacel SVC2475 Ref SVC2475
Mobi-tools glide TMG6410 Ref TMG6410
Mobi-tools translide TTE6110 Ref TTE6110
Salvafix Transit SVF3370 Ref SVF3370
Salvaclip SCP4330 Ref SCP4330
Salvacel SVC2500 Ref SVC2500
Salvacel SVC2476XL Ref SVC2476XL
Salvacel SVC2200 Ref SVC2200
Salvafix Standard SVF3322 Ref SVF3322
Medi-Roller Pro TMR6255 Ref TMR6255
Medi-Roller TMR6252 Ref TMR6252
Salvaclip Comfort SCC4216 Ref SCC4216
Salvaclip SCP4275 Ref SCP4275
Salvafix Memory PRO SVF3350 Ref SVF3350
Mobi-tools Slide TMS6335 Ref TMS6335
Salvaclip Comfort SCC4316 Ref SCC4316
Salvacel SVC2590 Ref SVC2590
Salvafix Transit SVF3478 Ref SVF3478
Salvaclip SCP4275L Ref SCP4275L
Salvacel SVC2300 Ref SVC2300
Salvaclip Safe SCF4465 Ref SCF4465
Salvafix Transit SVF3480 Ref SVF3480
Mobi-tools Slide TMS6345 Ref TMS6345
Salvaclip Safe SCF4456 Ref SCF4456
Mobi-tools translide TTE6142 Ref TTE6142
Showing 1-50 of 134
FDA establishments
- Medi Care System S.L.U. Mataro Barcelona · ES FEI 3008797789
What MEDI CARE SYSTEM SLU makes
The company manufactures reusable and single-use devices designed to assist with patient mobility, restraint, and transfer. These include occupant restraints and supports for wheelchairs and standers, limb/torso/head restraints, sliding boards and mats for patient transfers, patient lifting belts and harnesses, position turntables, and assistive nightwear.
All listed devices fall under Class I classification in the FDA’s UDI system, ensuring compliance with regulatory requirements for low-risk medical devices. The portfolio is registered in the FDA’s Unique Device Identifier (UDI) database, reflecting their availability in the United States.
Frequently asked questions
What types of medical devices does Medi Care System SLU manufacture?
Medi Care System SLU specializes in devices that support patient mobility, restraint, and safe transfers. Their portfolio includes reusable and single-use products like wheelchair occupant restraints and supports, limb/torso/head restraints, patient transfer sliding boards and mats, manual lifting belts/harnesses, position turntables, and assistive nightwear. These devices are designed to enhance patient care and safety during movement and positioning.
Where is Medi Care System SLU based, and where are their devices available?
Medi Care System SLU is based in the United States. Their devices are registered in the FDA’s Unique Device Identifier (UDI) database, indicating their availability and regulatory compliance within the U.S. market. This registration reflects their presence in the American healthcare system.
Which regulatory registries list Medi Care System SLU’s devices?
Medi Care System SLU’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a global standard for identifying medical devices, ensuring traceability and regulatory oversight. Listing in this database confirms the devices meet FDA requirements for classification and availability in the U.S.
How are Medi Care System SLU’s devices classified under FDA regulations?
All of Medi Care System SLU’s listed devices fall under Class I classification in the FDA’s UDI system. Class I devices are considered the lowest risk to patients and generally do not require pre-market approval, though they must still comply with FDA registration, labeling, and manufacturing standards. This classification aligns with their focus on mobility aids, restraints, and transfer tools, which are designed for minimal risk when used as intended.
Information
- Country
- US
- Website
- medisystemsl.com
- [email protected]
- Phone
- +34937570049
- DUNS number
- 511139446