Easy@Home Electronic Pulse Stimulator

FDA UDI

Class II (US FDA UDI)

by Easy Healthcare Corporation

Identity

Trade Name: Easy@Home Electronic Pulse Stimulator FDA UDI
Generic Name: Hand-held electric massager FDA UDI
Model / Reference: EHE015BLE FDA UDI

Identifiers

Primary DI / UDI-DI: 00810038633947 FDA UDI
FDA Product Code: NUH FDA UDI
NGX FDA UDI
IRT FDA UDI
NYN FDA UDI
GMDN Term: Hand-held electric massager FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.5890 FDA UDI
890.5850 FDA UDI
890.5740 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

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand-held electric massager

Easy@Home Electronic Pulse Stimulator by Easy Healthcare Corporation — 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: Easy Healthcare Corporation

Sources (1)

FDA UDI 4de2d095-5c19-41f3-91dd-c7fe5da59dfd 32 fields · synced Jun 1, 2026