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Ad Rem Technology Sarl

France · Paris
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Brazil, Canada, Singapore, Hong Kong, Russia — 6 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
2510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class II 2
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
6active device licences
Class II 6
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
2device registrations
CLASS B 2
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
1valid listings
Class II 1
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
1active registrations
Class 2a 1
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 States0 registration records, 2 510(k), 0 PMA
Brazil2 confirmed, 2 excluded
Canada6 confirmed, 0 excluded
Manufacturer names merged into this page: AD REM TECHNOLOGY · AD REM TECHNOLOGY SARL

Company information

Country
France
City
Paris

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

12008 · K072252
12015 · K141919

Registration details (sample)

MarketIdentifierNameClass / date
USK141919VEINOPLUS SPORT NEUROMUSCULAR STIMULATOR2015-06-16
USK072252VEINOPLUS NEUROMUSCULAR STIMULATOR2008-01-30
BR80524240005VEINOPLUS BACKClass II
BR80524240004VEINOPLUSClass II
CA83747VEINOPLUS VI MODEL 2.1Class II
CA83749VEINOPLUS PACKClass II
CA90026VEINOPLUS DVT - MODEL 2.1Class II

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