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Advanced Sound Unit

FDA UDI

Class II (US FDA UDI)

by Paramount Bed Co., Ltd.

Identity

Trade Name
Advanced Sound Unit FDA UDI
Generic Name
Loudspeaker FDA UDI
Device Name
Electrical Hospital Bed Accessory to be used for providing notification to a patient and intended users FDA UDI
Model / Reference
NS-S10U FDA UDI
Description
Electrical Hospital Bed Accessory to be used for providing notification to a patient and intended users FDA UDI

Identifiers

Primary DI / UDI-DI
04527799703678 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Loudspeaker 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Loudspeaker

Advanced Sound Unit by Paramount Bed Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32d7e629-9c76-4da0-8e44-373148c2e928 33 fields · synced May 30, 2026