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Klyo

FDA UDI

Class I (US FDA UDI)

by Klyo Medical Systems Inc

Identity

Trade Name
KLYO FDA UDI
Generic Name
Manual hospital bed FDA UDI
Device Name
A mechanical bed designed to be used as a patient bed for rest/sleep in a hospital ward/room with manual mechanisms to adjust the height and surface contour of the bed. It typically includes a framework with wheels, a mattress support platform that can articulate, a headboard and footboard, siderails, and mechanical manually-operated controls to operate the bed. FDA UDI
Model / Reference
KMHBD FDA UDI
Description
A mechanical bed designed to be used as a patient bed for rest/sleep in a hospital ward/room with manual mechanisms to adjust the height and surface contour of the bed. It typically includes a framework with wheels, a mattress support platform that can articulate, a headboard and footboard, siderails, and mechanical manually-operated controls to operate the bed. FDA UDI

Identifiers

Primary DI / UDI-DI
B773KMHBD0 FDA UDI
FDA Product Code
FNJ FDA UDI
GMDN Term
Manual hospital bed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual hospital bed

Klyo by Klyo Medical Systems Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual hospital bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76aac46d-ff3d-4529-95db-443c45faac2b 34 fields · synced May 30, 2026