Hertart
Country not established
- Devices
- 4
What Hertart makes
Hertart manufactures sterile, single-use culture dishes designed for laboratory cell and tissue culture applications. Their products include standard petri dishes (40 mm and 60 mm), multi-well dishes (5-well, 9-well, and 16-well formats), and specialized variants such as micro droplet dishes and centre well dishes for assisted reproductive techniques like ICSI.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States, adhering to applicable regulatory standards for in vitro diagnostic and laboratory equipment.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hertart have in the registry?
The registry currently lists 4 devices for Hertart. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hertart's devices?
Among its 4 most recently registered devices, Hertart has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Hertart's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Hertart's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hertart in the registry?
The most recently registered devices listed for Hertart include Micro well group culture dish, 9-well 16604, Micro well group culture dish, 16-well 16606, Micro well group culture dish, 9-well; Micro well group culture dish, 16-well and CULTURE DISH 40 MM, CULTURE DISH 60 MM, MICRO DROPLET CULTURE DISH, 5 WELL CULTURE DISH, CENTRE WELL DISH, ICSI DISH.