HomeMexicoCOMPANIA MEXICANA DE RADIOLOGIA CGR, S.A. DE C.V.

COMPANIA MEXICANA DE RADIOLOGIA CGR, S.A. DE C.V.

Mexico · Queretaro
✓ Record-verifiedregistrations found in 1 markets

This company has registrations in United States — 1 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
6listed device types
Class I 3Class II 3Class III 0
plus 8 registration records and 4 510(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
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 States8 registration records, 4 510(k), 0 PMA
Manufacturer names merged into this page: COMPANIA MEXICANA DE RADIOLOGIA CGR, S.A. DE C.V.

Company information

Country
Mexico
City
Queretaro

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

12013 · K123650
12016 · K161518
12018 · K182134
12020 · K193637

FDA listed device types

System, Image Processing, Radiological 1System, X-Ray, Stationary 1Table, Radiologic 1Holder, Radiographic Cassette, Wall-Mounted 1Generator, High-Voltage, X-Ray, Diagnostic 1Tube Mount, X-Ray, Diagnostic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK193637MRH ALFA Radiographic System, MRH II Radiographic System, MRH IIE Radiographic System2020-01-28
USK182134ARiX RAD Radiographic System2018-11-26
USK161518PACS CORE/ENCORE2016-08-17

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