FDA.reportPublic FDA data

Teleflex Medical Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30124815353012481535Teleflex Medical Inc.1N2026-01-014300 Glendale Milford Road Cincinnati OH US 45242
14174111417411Teleflex Medical Inc.1N2020-04-25900 W. University Drive, ARLINGTON HEIGHTS IL US 60004

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
228271162764027K993355HUDSON RCI CONCHA COLUMN, CAT. NO. 385-40 AND HUDSON RCI CIRCUIT, CAT. NO. 780-40, 780-41, 780-42, 780-43BTT2000-05-24
228272052873976K834151CONCHATHERM LHF HUMIDIFIER HEATERBTT1984-01-13
228271266009555K833974AQUAPAK 020 HUMIDIFIER ADAPTERBTT1983-12-16
228272050444580K820878CONCHO PEDIATRIC PACKBTT1982-05-03
228271688576668K780845CONCHANEOPAK A CARTRIDGE HUMIDIFIERBTT1978-08-14
228272069609347K780562AQUAPAK PREFILLED HUMIDIFIERBTT1978-04-27
228271417687927K772348NEBULIZER ADAPTERCAF1978-01-03
228271715641495K760866CONCHA-COLUMNBTT1976-11-01
3133401563198037K231603Standard Staple-Line Reinforcement (SSLR23)OXC2023-10-06
3133401363642130K222085Standard Tapered Bougie, 38 Fr.KNT2022-10-31
3133401016278107K210278Titan SGSGDW2021-04-28
3133401769300363K200517Standard TrocarGCJ2020-04-09
228271872474299K153010Hudson RCI AquaPak Sterile Prefilled NebulizersCAF2016-07-26
228271179632630K142153HUDSON RCI ADDIPAK UNIT DOSE VIAL, 0.9% FULL NORMAL SALINE SOLUTION, 3ML;5ML;15MLCAF2015-04-29
228271858852026K141353HUDSON RCI AQUAPAK HUMIDIFIER ADAPTORBTT2014-08-01
228271764623000K141214AQUAPAK NEBULIZER ADAPTORS/RESERVOIRSCAF2014-12-18
228271151495191
228271344165363
228271352442166

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
BTT82014-08-01
CAF42016-07-26
OXC12023-10-06
KNT12022-10-31
GDW12021-04-28
GCJ12020-04-09