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L I N E T spol. s r.o.

US

Last updated May 27, 2026

What L I N E T spol. s r.o. makes

The company manufactures a range of hospital and home beds, including basic electric hospital beds, kinetic beds, and powered birthing tables. Their portfolio also includes alternating-pressure mattress overlays, manual patient transfer systems, and paediatric-specific beds, as well as manual hospital stretchers for patient movement.

These devices are classified under FDA regulations as Class I or Class II and are listed in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States, adhering to applicable U.S. medical device compliance requirements.

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 L I N E T spol. s r.o. manufacture?

L I N E T spol. s r.o. specializes in a variety of hospital and home-use beds and related patient support systems. Their product range includes basic electric hospital beds, kinetic beds designed for repositioning patients, and powered birthing tables for obstetric use. They also produce alternating-pressure mattress overlays to prevent pressure ulcers, manual patient transfer systems for safe movement, paediatric beds tailored for children, and manual hospital stretchers for transporting patients. These devices are engineered to support clinical care in both acute and home care settings.

Where is L I N E T spol. s r.o. based, and does this affect their device compliance?

L I N E T spol. s r.o. is based in the United States, which means their devices must comply with U.S. medical device regulations, including those set by the FDA. The company’s products are designed and manufactured to meet applicable U.S. requirements, ensuring they align with regulatory expectations for safety, performance, and quality. Compliance is determined on a device-by-device basis, as individual products may fall under different classification rules.

Which regulatory registries or databases list L I N E T spol. s r.o.’s devices?

L I N E T spol. s r.o.’s devices are included in the FDA’s Unique Device Identification (UDI) system. The UDI system assigns a unique product identifier to each device, enabling better tracking, traceability, and transparency in the healthcare supply chain. This listing helps healthcare providers, regulators, and other stakeholders verify and manage the devices in use.

How are L I N E T spol. s r.o.’s devices classified under FDA regulations?

L I N E T spol. s r.o.’s devices are classified under the FDA’s system as either Class I or Class II. Class I devices generally pose the lowest risk and may be subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on factors like the device’s intended use, potential risks, and the body system it interacts with, as outlined in the FDA’s regulatory framework.

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

Information

Country
US
Address
—
Website
linet.cz
LinkedIn
—
Facebook
—
Phone
+420312576400
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
644544504

Catalogue (253)

Page 5 of 6
DeviceModel / ReferenceRegistriesClassStatus
sentida 03 1WIS13263543101
FDA UDI
Class IIActive
Eleganza 5 1GE512055-45
FDA UDI
Class IIActive
sentida 03 1WIS13283543101
FDA UDI
Class IIActive
Ave 2 4BCPPB-BCZ0009
FDA UDI
Class IIUnknown
Eleganza 4 1GE412055-1081
FDA UDI
Class IIActive
Eleganza 4 1GE412055-291
FDA UDI
Class IIActive
Eleganza 4 1GE412055-1376
FDA UDI
Class IIActive
Multicare X 1MCX12050-906
EUDAMEDFDA UDI
Class IIActive
Multicare 1MC17350-1471
FDA UDI
Class IIActive
Eleganza 3 1GZ6A100-32
FDA UDI
Class IIActive
Protevo AF10MCM-VC-35868
FDA UDI
Class IIActive
Protevo AF10-LM-35858
FDA UDI
Class IIActive
OptiCare 1VSR00025A000
FDA UDI
Class IIActive
Protevo AF8-TC-35837
FDA UDI
Class IIActive
Sprint 100 1ES105409-3
FDA UDI
Class IIActive
sentida 03 1WIS13233543101
FDA UDI
Class IIActive
Symbioso 250 1VSK0B0006000
FDA UDI
Class IIActive
OptiCare 1VSK0B000A000
FDA UDI
Class IIActive
Protevo AF10MCM-TC-35837
FDA UDI
Class IIActive
Ave 2 1PPBA4-619
FDA UDI
Class IIActive
Eleganza 3 1GZ6A100-28
FDA UDI
Class IIActive
Eleganza 3 1GZ6A100-40
FDA UDI
Class IIActive
Multicare 1MC17350-647
FDA UDI
Class IIActive
Eleganza 4 1GE412055-1197
FDA UDI
Class IIActive
Tom 2 1K41B511-10
EUDAMEDFDA UDI
Class IIActive
Eleganza 5 1GE512055-928
FDA UDI
Class IIActive
Eleganza 5 1GE512055-988
FDA UDI
Class IIActive
Tom 2 1K5B554-3
FDA UDI
Class IIActive
Eleganza 4 1GE412055-314
FDA UDI
Class IIActive
Multicare 1MC17350-718
FDA UDI
Class IIActive
Tom 2 1K41B511-18
FDA UDI
Class IIActive
Vibwife 1VBBA-17
FDA UDI
Class IIActive
Eleganza 4 1GE412055-383
FDA UDI
Class IIActive
Ave 2 4BCPPB-ACZ001
EUDAMEDFDA UDI
Class IIActive
Sprint 100 1ES15301-3
FDA UDI
Class IIActive
Eleganza 5 1GE512055-1004
FDA UDI
Class IIActive
Multicare 1MC17350-735
FDA UDI
Class IIActive
Eleganza 5 1GE512055-41
FDA UDI
Class IIActive
Ave 2 4BCMPPBAT00002
FDA UDI
Class IIActive
Symbioso 1VSM00025Y000
FDA UDI
Class IIActive
Multicare 1MC17350-2323
FDA UDI
Class IIActive
Sprint 100 1ES105409-63
FDA UDI
Class IIActive
Symbioso 250 1VSR000276000
FDA UDI
Class IIActive
Sprint 100 1ES10002
FDA UDI
Class IIActive
Vibwife 1VBBA-10
FDA UDI
Class IIActive
Eleganza 5 1GE512055-1
FDA UDI
Class IIActive
Protevo AF10MCM-LM-35858
FDA UDI
Class IIActive
Tom 2 1K5B554-9
FDA UDI
Class IIActive
Multicare 1MC5A650-282
FDA UDI
Class IIActive
Eleganza 5 1GE512055-932
EUDAMEDFDA UDI
Class IIActive

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Authorities

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FDA Establishments (1)

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

  • LINET spol. s r.o. Slany Stredocesky Kraj · CZ FEI 3008058231