Cardiotech Intl.
Country not established
- Devices
- 1
What Cardiotech Intl. makes
Cardiotech Intl. manufactures the Cardiotech Antibiotic Hydrogel Wound Dressing, a topical hydrogel designed to deliver antimicrobial agents directly to wound sites for infection management.
The company’s portfolio is regulated under FDA Class II (U) devices and is listed in the FDA 510(k) registry. The manufacturer is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cardiotech Antibotic Hydrogel Wound Dressing Ref K022584
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardiotech Intl. have in the registry?
The registry currently lists 1 device for Cardiotech Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardiotech Intl.'s devices?
Among its 1 most recently registered device, Cardiotech Intl. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Cardiotech Intl. in the registry?
The most recently registered devices listed for Cardiotech Intl. include CARDIOTECH ANTIBOTIC HYDROGEL WOUND DRESSING.