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 Number: 3011787398
• FEI Number: 3011787398
• Name: Maureen OConnell
• Owner & Operator: Beneli AB
• Contact Address: Porfyrgatan 5 ; Helsingborg SE-M Skane lan [SE-12] 25468 SE
• Official Correspondent:
  • Jenny Elvstrand
  • 46-42-256016-x
• US Agent:
  • Maureen OConnell
  • OConnell Regulatory Consultants, Inc.
  • 978 2071245
  • maureen@oconnellregulatory.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 44 Oak Street ; Stoneham, MA 02180 US
• Establishment Type: Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
DRX Maureen OConnell [Beneli AB]	Universal Patch	2015-06-08
DRX Maureen OConnell [Beneli AB]	Snap Strip	2015-06-08
DRX Maureen OConnell [Beneli AB]	Patch	2015-06-08
DRX Maureen OConnell [Beneli AB]	Patch electrode	2015-06-08
DRX Maureen OConnell [Beneli AB]	MCOT patch	2015-06-08
DRX Maureen OConnell [Beneli AB]	Fast Fix ECG Electrode	2015-06-08
DRX Maureen OConnell [Beneli AB]	BodyGuardian Mini Strip	2015-06-08