Mt Derm G M B H

FDA Filings

This page includes the latest FDA filings for Mt Derm 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 Number3006634874
FEI Number3006634874
NameMT.DERM GmbH
Owner & OperatorMT.DERM GmbH
Contact AddressGustav-Krone-Strasse 3
Berlin DE-BE Berlin 14167 DE
Official Correspondent
  • Paco Pelt
  • 49-30-845885-601
US Agent
Importing Logistics Registration
ImporterAMIEA MED, INC
Address111 North Orange Avenue Suite 775
Orlando, FL 32801 UNITED STATES
Email Addressinfo@us.amieamed.com
Phone1 407 4970909 233
FAX1 30 84588555
Importer TypeAgent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressGustav-Krone-Strasse 3
Berlin Berlin, 14167 DE
Establishment Type
  • Manufacture Medical Device
  • Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device
Company
DeviceDate
MT.DERM GmbH
 Safety Needle Cartridge 6-MNP 1.5 Exceed US 2020-01-09
MT.DERM GmbH
 Footswitch 2020-01-09
MT.DERM GmbH
 Exceed 2020-01-09
MT.DERM GmbH
 Safety Needle Cartridge 6-MNP 1.5 Exceed US EMNPAED06USMP2019-07-24
MT.DERM GmbH
 Footswitch E100201USMP 2019-07-24
MT.DERM GmbH
 Footswitch E100201USMP 2019-07-24
MT.DERM GmbH
 Exceed AD61USMP2019-07-24
MT.DERM GmbH
 Exceed AD61USMP2019-07-24
MT.DERM GmbH
Safety needle Cartridge 6-MNP 1.5 Exceed US2019-07-22
MT.DERM GmbH
Footswitch2019-07-22
MT.DERM GmbH
Exceed2019-07-22
Mt. Derm GmbH
Exceed Microneedling Device2019-07-19
MT.DERM GmbH
Safety needle Cartridge 6-MNP 1.5 Exceed US2018-10-08
MT.DERM GmbH
Footswitch2018-10-08
MT.DERM GmbH
Exceed2018-10-08
MT.DERM GmbH
Exceed Microneedling Device2018-09-07

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