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Home Care

FDA UDI

Class II (US FDA UDI)

by Home Care Technology Co., Ltd.

Identity

Trade Name
Home Care FDA UDI
Generic Name
Electrical probe/electrode conductive pad FDA UDI
Device Name
Transcutaneous electrical stimulation electrode FDA UDI
Model / Reference
FA5050 FDA UDI
Description
Transcutaneous electrical stimulation electrode FDA UDI

Identifiers

Primary DI / UDI-DI
04719873684755 FDA UDI
510(k) Number
K022917 FDA UDI
FDA Product Code
GXY FDA UDI
GMDN Term
Electrical probe/electrode conductive pad FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1320 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrical probe/electrode conductive pad

Home Care by Home Care Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical probe/electrode conductive pad.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ea4d8ba5-809f-4ad3-b8ba-9f774a4f34fc 34 fields · synced May 30, 2026