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Homedics

FDA UDI

Class I (US FDA UDI)

by Health Care Massage Branch of Zhangzhou Easepal Industrial Co., Ltd.

Identity

Trade Name
Homedics FDA UDI
Generic Name
Hand-held electric massager FDA UDI
Device Name
THERA-P BODY MASSAGER WITH FDA UDI
Model / Reference
HHP-110J-CVS FDA UDI
Description
THERA-P BODY MASSAGER WITH FDA UDI

Identifiers

Primary DI / UDI-DI
00031262080790 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

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: Hand-held electric massager

Homedics by Health Care Massage Branch of Zhangzhou Easepal Industrial Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Health Care Massage Branch of Zhangzhou Easepal Industrial Co., Ltd.

Sources (1)

  • FDA UDI 0da8c415-fed3-4d34-b68a-6b0974252078 33 fields · synced May 30, 2026