Multicare

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name: Multicare FDA UDI
Generic Name: Kinetic bed FDA UDI
Device Name: Electrically operated hospital bed. FDA UDI
Model / Reference: 1MC17350-502 FDA UDI
Description: Electrically operated hospital bed. FDA UDI

Identifiers

Primary DI / UDI-DI: 08592654095898 FDA UDI
FDA Product Code: IOQ FDA UDI
GMDN Term: Kinetic bed FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5170 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Kinetic bed

Multicare by L I N E T spol. s r.o. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

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

Sources (1)

FDA UDI 663c9106-6dbd-4b36-9234-74a369602d4f 33 fields · synced Jun 8, 2026