Teleflex Medical Oem

FDA Filings

This page includes the latest FDA filings for Teleflex Medical Oem. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005232773
FEI Number3005232773
NameTeleflex Medical OEM
Owner & OperatorTeleflex
Contact Address3015 Carrington Mill Blvd.
Morrisville NC 27560 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3750 Annapolis Ln N Ste 160
Plymouth, MN 55447 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)



FDA Filings

Device
Company
DeviceDate
Teleflex Medical OEM [Teleflex]
Uro Pass Ureteral Access Sheath2013-07-02
Teleflex Medical OEM [Teleflex]
Uro-Pass2013-01-08

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.