Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004753827

FEI Number

3004753827

Entity Name

EVERLIFE MEDICAL EQUIPMENT CO., LTD.

City/State/Country

New Taipei City, TW

Establishment Address

8F, No. 8, Lane 235, Bao-Qiao Road, Xin-Dian District, New Taipei City 23145, TW

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

EVERLIFE MEDICAL EQUIPMENT CO., LTD. (Owner Number: 9066394)

Owner / Operator Contact Address

8th Floor, No. 8, Lane 235, Bao-Qiao Road, Xin-Dian District, New Taipei City, TW-TPE 23145, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Flex-TENS EVERLIFE EVERLIFE EVERLIFE EVERLIFE Dysphagia Therapy Unit Electrode Lead Wires EVERLIFE Flex-MT

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2015-01-06
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2008-03-28
GXY	Electrode, Cutaneous	Neurology	Class 2	882.1320	2007-12-02
LIH	Interferential Current Therapy	Neurology	Class 2	882.5890	2007-12-02
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2007-12-02
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2017-02-20
IKD	Cable, Electrode	Physical Medicine	Class 2	890.1175	2011-07-26
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief	Neurology	Class 2	882.5890	2015-01-06
IPF	Stimulator, Muscle, Powered	Physical Medicine	Class 2	890.5850	2015-01-06

Official Correspondent

No official correspondent registered.

US Agent Details

Shu-Chen Cheng Business: ROC Chinese-European Industrial Research Society Email: ceirs.jen@msa.hinet.net Phone: (614) 5888168

Related Public Records

Same Entity

EVERLIFE MEDICAL EQUIPMENT CO., LTD.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K122948	Gemore Technology Co, Ltd.	GEM-STIM COMBO STIMULATOR	2012-12-21
K033455	Biomedical Life Systems, Inc.	ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5	2004-01-15
K810593	Medical Devices, Inc.	NEUROPAC ULTRA I	1981-03-13
K070612	Top-Rank Health Care Equipment Co., Ltd.	TOP-RANK ADHESIVE ELECTRODE	2007-05-07
K123915	Grass Technologies, an Astro-Med, Inc. Product Gro	DE48-PLUS	2013-04-24

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004753827. Last updated year: 2026. Please use registration number 3004753827 when referencing this establishment in official correspondence.