Lauer Ltd., Hong Kong
GermanyFDA applicant, unverified
- Devices
- 1
What Lauer Ltd., Hong Kong makes
Lauer Ltd. manufactures the AQUABOSS ECORO DIA 50, a medical device designed for endoscopic procedures, specifically for tissue ablation or resection within the biliary or pancreatic ducts.
The AQUABOSS ECORO DIA 50 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in Hong Kong with regulatory submissions filed in the United States.
Catalogue
Aquaboss Ecoro Dia 50 Ref K032004
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lauer Ltd., Hong Kong have in the registry?
The registry currently lists 1 device for Lauer Ltd., Hong Kong. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lauer Ltd., Hong Kong's devices?
Among its 1 most recently registered device, Lauer Ltd., Hong Kong has devices listed in FDA 510(k) (1 device).
What risk classes do Lauer Ltd., Hong Kong's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lauer Ltd., Hong Kong's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lauer Ltd., Hong Kong in the registry?
The most recently registered devices listed for Lauer Ltd., Hong Kong include AQUABOSS ECORO DIA 50.