Hertart Aps
Country not established
- Devices
- 1
What Hertart Aps makes
Hertart Aps manufactures the Pasteur Pipette 3mL, a glass pipette designed for precise liquid handling in laboratory settings.
The Pasteur Pipette 3mL is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in Sweden.
Catalogue
Pasteur Pipette 3mL Ref K201213
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 305164017
Frequently asked questions
How many devices does Hertart Aps have in the registry?
The registry currently lists 1 device for Hertart Aps. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hertart Aps's devices?
Among its 1 most recently registered device, Hertart Aps has devices listed in FDA 510(k) (1 device).
What risk classes do Hertart Aps's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hertart Aps's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hertart Aps in the registry?
The most recently registered devices listed for Hertart Aps include Pasteur Pipette 3mL.