HomeUSACovidien Iic

Covidien Iic

USA · Mansfield
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Singapore, Hong Kong, Israel — 5 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
1510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
43registered devices
Class I 4Class II 39
53 including historic records
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
10device registrations
CLASS B 3CLASS C 6CLASS D 1
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
1valid listings
Class III 1
ILIsraelAMAR
6registrations
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 States0 registration records, 1 510(k), 0 PMA
Brazil43 confirmed, 0 excluded
Manufacturer names merged into this page: COVIDIEN IIC, MANSFIELD · COVIDIEN IIc

Company information

Country
USA
City
Mansfield

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

12014 · K141357

Registration details (sample)

MarketIdentifierNameClass / date
USK141357BARRX FLEX RFA ENERGY GENERATOR2014-08-21
BR10349000123CATETER PERITONEAL CURL CATH QUINTONClass II
BR10349000075VISIPORT - TROCARTE OPTICO DESCARTAVEL COM CANULAAUTO SUTUREClass II
BR10349000004VERSAPORT CÂNULA E TROCARTE DESCARTÁVEL AUTO SUTUREClass II

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