Beneli Ab

FDA Filings

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

FDA Registration(s)
Registration Number3011787398
FEI Number3011787398
NameMaureen OConnell
Owner & OperatorBeneli AB
Contact AddressPorfyrgatan 5
Helsingborg SE-M Skane lan [SE-12] 25468 SE
Official Correspondent
  • Jenny Elvstrand
  • 46-42-256016-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address44 Oak Street
Stoneham, MA 02180 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
Maureen OConnell [Beneli AB]
Universal Patch2015-06-08
Maureen OConnell [Beneli AB]
Snap Strip2015-06-08
Maureen OConnell [Beneli AB]
Patch2015-06-08
Maureen OConnell [Beneli AB]
Patch electrode2015-06-08
Maureen OConnell [Beneli AB]
MCOT patch2015-06-08
Maureen OConnell [Beneli AB]
Fast Fix ECG Electrode2015-06-08
Maureen OConnell [Beneli AB]
BodyGuardian Mini Strip2015-06-08

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