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Handheld controller

FDA UDI

Class II (US FDA UDI)

by Paramount Bed Co., Ltd.

Identity

Trade Name
Handheld controller FDA UDI
Generic Name
Bed remote control FDA UDI
Device Name
Controller for physicians, nurses and a patient to operate the bed. FDA UDI
Model / Reference
RC-1850U FDA UDI
Description
Controller for physicians, nurses and a patient to operate the bed. FDA UDI

Identifiers

Primary DI / UDI-DI
04527799700400 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Bed remote control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bed remote control

Handheld controller by Paramount Bed Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed remote control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 44d37324-9071-410c-8710-7d8501bb5434 33 fields · synced May 30, 2026