Womed SAS
Country not established FDA
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Womed SAS makes
Womed Sas manufactures the Womed Leaf Resorbable Adhesion Barrier, a medical device designed to prevent postoperative adhesions in surgical procedures. This product is intended for use in abdominal and pelvic surgeries to reduce tissue bonding and complications.
The Womed Leaf Resorbable Adhesion Barrier is classified as a Class III device under FDA regulations and is listed under a Premarket Approval (PMA). The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Womed Leaf Resorbable Adhesion Barrier Ref P240015
Regimes: CE MDR PMA Registry: PMA
FDA establishments
- Womed SAS Montpellier Herault · FR FEI 3031365458
Frequently asked questions
How many devices does Womed Sas have in the registry?
The registry currently lists 4 devices for Womed Sas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Womed Sas's devices?
Among its 4 most recently registered devices, Womed Sas has devices listed in FDA PMA (1 device) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Womed Sas's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Womed Sas's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from Womed Sas in the registry?
The most recently registered devices listed for Womed Sas include Womed Leaf LEAF-S, Womed Leaf LEAF-M, Womed Leaf LEAF-L and Womed Leaf Resorbable Adhesion Barrier.
Which FDA establishments are linked to Womed Sas?
1 FDA establishment is linked to Womed Sas in the registry; they are listed on the company page.