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Homedics

FDA UDI

Class I (US FDA UDI)

by Zhangzhou Easepal Innovation Co., Ltd.

Identity

Trade Name
Homedics FDA UDI
Generic Name
Hand-held electric massager FDA UDI
Device Name
Eye Massager FDA UDI
Model / Reference
SPE-110H-2 FDA UDI
Description
Eye Massager FDA UDI

Identifiers

Primary DI / UDI-DI
00031262107213 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Hand-held electric massager FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

Yes

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: Hand-held electric massager

The Homedics Hand-held Electric Massager is a versatile and effective tool for relieving muscular tension, reducing arthritic pain, and improving joint mobility. This portable device uses vibrations and heat to target specific areas of the body, making it an excellent option for both home and healthcare applications.

Similar devices

Also classified as Hand-held electric massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 787f6160-dea7-4001-8311-8e685d1a484c 33 fields · synced Jul 20, 2026