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Home›Taiwan›EVERLIFE MEDICAL EQUIPMENT CO., LTD.

EVERLIFE MEDICAL EQUIPMENT CO., LTD.

Taiwan · New Taipei City
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
pendingnot queried
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
5listed device types
Class I 0Class II 5Class III 0
plus 9 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
2active device licences
Class II 2
4 including historic records
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States9 registration records, 3 510(k), 0 PMA, 1 excluded
Canada2 confirmed, 0 excluded
Manufacturer names merged into this page: EVERLIFE MEDICAL EQUIPMENT CO., LTD.

Company information

Country
Taiwan
City
New Taipei City

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

32007 · K071624

FDA listed device types

Stimulator, Muscle, Powered 1Cable, Electrode 1Electrode, Cutaneous 1Interferential Current Therapy 1Stimulator, Nerve, Transcutaneous, For Pain Relief 1

Registration details (sample)

MarketIdentifierNameClass / date
USK071624EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR2007-11-27
USK071320EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-2013112007-08-17
USK070890EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-1005072007-06-29
CA93426ELECTRODES FOR TENS & EMSClass II
CA92044EVERMICROClass II

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