HomeFranceLamidey Noury Medical

Lamidey Noury Medical

France · Verrieres Le Buisson Essonne
✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, Taiwan, Singapore, Australia, Israel, 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
4listed device types
Class I 0Class II 4Class III 0
plus 2 registration records and 2 510(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
0active device licences
TWTaiwanTFDA
2valid device licences
Class II 2
SGSingaporeHSA SMDR
1device registrations
CLASS C 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
12active ARTG entries
Class I 5IIa 2IIb 5
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
3registrations
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 States2 registration records, 2 510(k), 0 PMA
Manufacturer names merged into this page: Lamidey Noury Medical

Company information

Country
France
City
Verrieres Le Buisson Essonne

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

12022 · K222542
12024 · K240504

FDA listed device types

Electrosurgical, Cutting & Coagulation & Accessories 1Electrode, Electrosurgical, Active, Urological 1Unit, Electrosurgical, Endoscopic (With Or Without Accessories) 1Resectoscope, Working Element 1

Registration details (sample)

MarketIdentifierNameClass / date
USK240504PLASMA EDGE System2024-06-12
USK222542MCB UNIT Model: V10GMCBUS2022-09-21

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