Mercan AB
Country not established
- Devices
- 2
What Mercan AB makes
Mercan AB manufactures reusable surgical drapes and nonsterile operating room/surgeons gowns designed for single-patient use in sterile procedures. The products are intended to maintain surgical site protection and reduce contamination risks during surgical interventions.
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
Mertex-Plus Reusable Surgical Drape Ref K012237
Regimes: 510(k) Registry: 510(k)Mertex-Plus O.R./Surgeons Gown, Nonsterile Ref K012240
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mercan AB have in the registry?
The registry currently lists 2 devices for Mercan AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mercan AB's devices?
Among its 2 most recently registered devices, Mercan AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Mercan AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mercan AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mercan AB in the registry?
The most recently registered devices listed for Mercan AB include MERTEX-PLUS REUSABLE SURGICAL DRAPE and MERTEX-PLUS O.R./SURGEONS GOWN, NONSTERILE.