Schmid Medizintechnik G M B H

FDA Filings

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

FDA Registration(s)

• Registration Number: 8010374
• FEI Number: 3005693456
• Name: Beate Weiss-Krull
• Owner & Operator: SCHMID MEDIZINTECHNIK GMBH
• Contact Address: ELTASTR.9 --; WURMLINGEN DE-BW Baden-Wurttemberg 78573 DE
• Official Correspondent:
  • ARTUR - SCHMID
  • 49-746-12723-x
• US Agent:
  • Beate Weiss-Krull
  • Beate Weiss-Krull, Attorney at Law
  • 503 2340355
  • bea@weisskrull-law.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 1050 SW 6th Ave., Suite 1100 ; Portland, OR 97204 US
• Establishment Type:
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
CCW Beate Weiss-Krull [SCHMID MEDIZINTECHNIK GMBH]	Laryngoscope	2016-08-25
GDZ Beate Weiss-Krull [SCHMID MEDIZINTECHNIK GMBH]	Handle	2016-07-20
FMH Beate Weiss-Krull [SCHMID MEDIZINTECHNIK GMBH]	Container	2016-04-13
GDG Beate Weiss-Krull [SCHMID MEDIZINTECHNIK GMBH]	Hook	1986-05-12