Novo Nordisk A S Needle Manufacturing Sourci

FDA Filings

This page includes the latest FDA filings for Novo Nordisk A S Needle Manufacturing Sourci. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 9681822
• FEI Number: 3004547341
• Name: NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI
• Owner & Operator: NOVO NORDISK INC.
• Contact Address: 800 Scudders Mill Road ; Plainsboro NJ 08536 US
• Official Correspondent:
  • John Signorin
  • x-609-9875967-x
• US Agent:
  • JOHN SIGNORIN
  • NOVO NORDISK INC.
  • 609 9875967 0
  • 609 9873916
  • JOHS@novonordisk.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: STENAGER ALLE 4 ; HJOERRING Region Nordjylland, -- DK
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN K173479 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NovoFine 32G Tip	2018-12-06
PMN K133738 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NovoFine? Plus	2014-05-30
PMN K133738 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NovoFine? Plus 32G x 4 mm (1/6") Disposable Needle	2014-05-30
PMN K090111 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NOVOFINE 32G Tip	2013-06-13
PMN K093109 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NovoTwist 32G Tip	2010-06-23
PMN K093109 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NovoTwist 30G	2010-06-23
PMN K050106 | FMI NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NOVOFINE AUTOCOVER 30G	2006-11-27
GAA NOVO NORDISK A/S - NEEDLE MANUFACTURING AND SOURCI [NOVO NORDISK INC.]	NOVOFINE 30G	1996-08-08