Gunter Martin G M B H Co Kg

FDA Filings

This page includes the latest FDA filings for Gunter Martin G M B H Co Kg. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 9680077
• FEI Number: 3002807123
• Name: GUNTER MARTIN GmbH & Co. KG
• Owner & Operator: GUNTER MARTIN GmbH & Co. KG
• Contact Address: HOLDERLINWEG 3 --; HAUSEN O.V. DE-BW Baden-Wurttemberg D-78595 DE
• Official Correspondent:
  • GUNTER - MARTIN
  • 49-7424-503210-x
• US Agent:
  • Franz Menean
  • MEDAGENT, Inc.
  • 603 5702039
  • 603 5702055
  • mail@medagent-usa.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: HOLDERLINWEG 3 ; HAUSEN O.V. Baden-Wurttemberg, D-78595 DE
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
KAK GUNTER MARTIN GmbH & Co. KG	PROBE	2000-11-08
JZF GUNTER MARTIN GmbH & Co. KG	SUCTION-TUBE	2000-11-08
JYG GUNTER MARTIN GmbH & Co. KG	CURETTE	2000-11-08
HNP GUNTER MARTIN GmbH & Co. KG	INTRODUCER CARTER S	2000-11-08
GEA GUNTER MARTIN GmbH & Co. KG	Cannula	2000-11-08
HNF GUNTER MARTIN GmbH & Co. KG	SCISSORS OPHTHALMIC	1996-02-14