Skip to content

MEDI CARE SYSTEM SLU

US Last updated 24 May 2026

Is this your brand? Sign in to claim this brand

Devices
134
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue134

Page 1 of 3

Showing 1-50 of 134

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • 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.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

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.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Phone
+34937570049
DUNS number
511139446