Annes Daye, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Annes Daye, Ltd. makes
Annes Daye, Ltd. manufactures the Daye Tampon, a menstrual hygiene product designed for internal use.
The Daye Tampon is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Daye Tampon Ref K223883
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Annes Daye, Ltd. have in the registry?
The registry currently lists 1 device for Annes Daye, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Annes Daye, Ltd.'s devices?
Among its 1 most recently registered device, Annes Daye, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Annes Daye, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Annes Daye, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Annes Daye, Ltd. in the registry?
The most recently registered devices listed for Annes Daye, Ltd. include Daye Tampon.