Duo-Med
Belgiumfrom SRN FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Duo-Med makes
Duo-Med makes surgical procedure packs, including those for hemicolectomy, gastric bypass, and sleeve gastrectomy. These products are used in specific medical procedures. The company's devices are focused on surgical applications.
The company's portfolio is regulated under Class IIb devices and is listed in the Eudamed registry. Duo-Med is based in Belgium. The devices are subject to regulatory oversight in the European Union.
Catalogue
Hemicolectomy left procedure pack Ref PP-LCOLON-5/7-01
CE MDR, withdrawn EUDAMEDGastric Bypass Procedure Pack Ref PP-GB-7/9-01
CE MDR, withdrawn EUDAMEDSleeve Gastrectomy Procedure Pack Ref PP-SG-8\10-01
CE MDR, withdrawn EUDAMED
FDA establishments
- Duomed, Inc. US
Frequently asked questions
How many devices does Duo-Med have in the registry?
The registry currently lists 3 devices for Duo-Med. Devices recorded under merged duplicate company entries are counted once.
Which registries list Duo-Med's devices?
Among its 3 most recently registered devices, Duo-Med has devices listed in EUDAMED (3 devices).
What risk classes do Duo-Med's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Duo-Med's devices are Class IIb. Each device page shows its own class and authorisation.
What are the newest devices from Duo-Med in the registry?
The most recently registered devices listed for Duo-Med include Hemicolectomy left procedure pack, Gastric Bypass Procedure Pack and Sleeve Gastrectomy Procedure Pack.
Which FDA establishments are linked to Duo-Med?
1 FDA establishment is linked to Duo-Med in the registry; they are listed on the company page.