EasyBoost

FDA UDI

Class II (US FDA UDI)

by Seneca Devices Inc

Identity

Trade Name: EasyBoost FDA UDI
Generic Name: Electrical assistive bed FDA UDI
Device Name: EasyBoost repositioning system compatible with HoverMatt. FDA UDI
Model / Reference: ESB-HM FDA UDI
Description: EasyBoost repositioning system compatible with HoverMatt. FDA UDI

Identifiers

Primary DI / UDI-DI: 00860004936831 FDA UDI
FDA Product Code: FNG FDA UDI
GMDN Term: Electrical assistive bed FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5500 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

FDA UDI

Category: Electrical assistive bed

EasyBoost by Seneca Devices Inc — 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: Seneca Devices Inc

Sources (1)

FDA UDI 151290e3-445f-45c5-afdf-c77961df886c 33 fields · synced Jun 8, 2026