Elos Medtech Microplast Ab

FDA Filings

This page includes the latest FDA filings for Elos Medtech Microplast 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: 3012416874
• FEI Number: 3012416874
• Name: Elos medtech Microplast AB
• Owner & Operator: Elos Medtech Microplast AB
• Contact Address: Hasthagsgatan 2 ; Skara SE-O Vastra Gotalands lan [SE-14] S-53237 SE
• Official Correspondent:
  • Maria Skold
  • 46-511-25700-x
• US Agent:
  • Jodie Gilmore
  • 901 3236699
  • Jodie.gilmore@elosmedtech.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Hasthagsgatan 2 ; Skara Vastra Gotalands lan [SE-14], S-532 37 SE
• Establishment Type: Manufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device Company	Device	Date
PMN K123641 | MQK Elos medtech Microplast AB	Micro Droplet Culture Dish	2016-03-02
PMN K123641 | MQK Elos medtech Microplast AB	ICSI Dish	2016-03-02
PMN K123641 | MQK Elos medtech Microplast AB	Culture Dish 40 mm	2016-03-02
PMN K123641 | MQK Elos medtech Microplast AB	Centre Well Dish	2016-03-02
PMN K123641 | MQK Elos medtech Microplast AB	5 Well Culture Dish	2016-03-02
PMN K150756 | MQK Elos medtech Microplast AB	Micro Well Group Culture Dish,9-well Micro Well Group Culture Dish,16-well	2016-03-01
PMN K150756 | MQK Elos medtech Microplast AB	Micro Well Group Culture Dish, 16-well	2016-03-01