Pertrach
Country not established
- Devices
- 2
What Pertrach makes
Pertrach manufactures emergency airway management kits, including modified adult cricothyroidotomy and percutaneous cricothyroidotomy kits designed for urgent surgical airway access.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Modified Adult Cricothyroidotomy Kit Ref K885139
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pertrach have in the registry?
The registry currently lists 2 devices for Pertrach. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pertrach's devices?
Among its 2 most recently registered devices, Pertrach has devices listed in FDA 510(k) (2 devices).
What risk classes do Pertrach's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Pertrach's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pertrach in the registry?
The most recently registered devices listed for Pertrach include MODIFIED ADULT CRICOTHYROIDOTOMY KIT and EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT, MODIF.