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Samarit Medical Industries Inc

US

Last updated May 25, 2026

What Samarit Medical Industries Inc makes

The company manufactures patient transfer sliding boards and mats, designed to assist healthcare providers in safely moving patients between surfaces like beds, stretchers, and wheelchairs. It also produces wheelchair seat cushions, which provide pressure relief and support for individuals with limited mobility. All products are branded under the Smart Rollboard line.

These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States, where its products are authorised for commercial distribution.

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 Samarit Medical Industries Inc manufacture?

Samarit Medical Industries Inc specialises in devices designed to aid patient mobility and comfort. Its primary products include patient transfer sliding boards and sliding mats, which help healthcare providers safely move patients between surfaces like beds, stretchers, and wheelchairs. Additionally, the company produces wheelchair seat cushions, which offer pressure relief and support for individuals with limited mobility. All products fall under the Smart Rollboard brand.

Where is Samarit Medical Industries Inc based, and where are its devices authorised for use?

Samarit Medical Industries Inc is based in the United States. The company’s devices are authorised for commercial distribution in the US, where they comply with applicable regulatory requirements. The specific devices are authorised individually, not the company itself.

How are Samarit Medical Industries Inc’s devices classified under FDA regulations?

Samarit Medical Industries Inc’s devices are classified as Class I under FDA regulations. This classification applies to low-risk devices that pose minimal potential harm to users, such as patient transfer aids and wheelchair cushions. The classification is determined by the device’s intended use and risk profile, as outlined in FDA guidelines.

Are Samarit Medical Industries Inc’s devices listed in any regulatory registries?

Yes, Samarit Medical Industries Inc’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain by assigning a unique identifier to each device, helping regulators, healthcare providers, and patients verify product details and compliance.

Why are all of Samarit Medical Industries Inc’s example devices named ‘Smart Rollboard’?

The company’s example devices are branded under the Smart Rollboard line, indicating they share a unified design philosophy focused on patient safety, ease of use, and mobility assistance. While the specific models may vary in features (e.g., sliding boards vs. cushions), the branding reflects a cohesive product family aimed at simplifying patient transfers and improving comfort for individuals with mobility needs.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
247963056

Catalogue (14)

DeviceModel / ReferenceRegistriesClassStatus
Smart Rollboard 4450
FDA UDI
Class IActive
Smart Rollboard 5260
FDA UDI
Class IActive
Smart Rollboard 4087
FDA UDI
Class IActive
Smart Rollboard 4100
FDA UDI
Class IActive
Smart Rollboard 4500
FDA UDI
Class IActive
Smart Rollboard 4400
FDA UDI
Class IActive
Smart Rollboard 4088
FDA UDI
Class IActive
Smart Rollboard 4010
FDA UDI
Class IActive
Smart Rollboard 4300
FDA UDI
Class IActive
Smart Rollboard 5248
FDA UDI
Class IActive
Smart Rollboard 4350
FDA UDI
Class IActive
Smart Rollboard 4460
FDA UDI
Class IActive
Smart Rollboard 4086
FDA UDI
Class IActive
Smart Rollboard 4014
FDA UDI
Class IActive

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