Hertart A P S

FDA Filings

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

FDA Registration(s)
Registration Number3008524469
FEI Number3008524469
NameBrett Glazar
Owner & OperatorHertART Aps
Contact AddressGustaf Werners gata 2
Vastra Frolunda SE-O Vastra Gotalands lan [SE-14] 42132 SE
Official Correspondent
  • Nina Arvidsson
  • 46-31-7218076-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3601 S Inca St
Englewood, CO 80110 US
Establishment Type
  • Manufacture Medical Device
  • Develop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Hertart ApS
Pasteur Pipette 3 mL 2020-12-30
Hertart ApS
Pasteur Pipette 1 mL 2020-12-30
HertART Aps
Pasteur Pipette 3mL, Pasteur Pipette 1mL2020-12-16
Hertart ApS
Centrifuge Tube 50 mL 2020-06-08
Hertart ApS
Centrifuge Tube 15 mL 2020-06-08
Hertart ApS
Oocyte Collection Tube 14 mL 2020-06-08
Hertart ApS
Collection Dish 90 mm 2020-06-08
Hertart ApS
ICSI Dish 2018-07-06
Hertart ApS
Centre Well Dish 2018-07-06
Hertart ApS
5 Well Culture Dish 2018-07-06
Hertart ApS
Micro Droplet Culture Dish 2018-07-06
Hertart ApS
Culture Dish 60 mm 2018-07-06
Hertart ApS
Culture Dish 40 mm 2018-07-06
Hertart ApS
Micro well group culture dish, 16-well 2018-07-06
Hertart ApS
Micro well group culture dish, 9-well 2018-07-06
Brett Glazar [HertART Aps]
Micro well group culture dish, 9-well Micro well group culture dish, 16 well2016-03-02
Brett Glazar [HertART Aps]
Micro Droplet Culture Dish2014-05-05
Brett Glazar [HertART Aps]
ICSI Dish2014-05-05
Brett Glazar [HertART Aps]
Culture Dish 60 mm2014-05-05
Brett Glazar [HertART Aps]
Culture Dish 40 mm2014-05-05
Brett Glazar [HertART Aps]
Centre Well Dish2014-05-05
Brett Glazar [HertART Aps]
5 Well Culture Dish2014-05-05

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