Pumuckl
Country not established
- Devices
- 1
What Pumuckl makes
Pumuckl manufactures disposable medical devices, including the PUMUCKL AND/OR DIETERLE, which are likely single-use items for clinical or procedural applications.
These devices are classified as Class I under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Pumuckl And/Or Dieterle Ref K904037
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pumuckl have in the registry?
The registry currently lists 1 device for Pumuckl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pumuckl's devices?
Among its 1 most recently registered device, Pumuckl has devices listed in FDA 510(k) (1 device).
What risk classes do Pumuckl's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pumuckl's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pumuckl in the registry?
The most recently registered devices listed for Pumuckl include PUMUCKL AND/OR DIETERLE.