Remeda AB
Active in EUDAMEDSwedenfrom SRN EUDAMED FDA SRN SE-MF-000003281 FEI 3013300766
- Devices
- 1
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
What Remeda AB makes
Remeda AB manufactures adjustable arm tables designed for hospital use, focusing on ergonomic support to reduce operator strain during procedures.
The company’s products fall under EU Class I medical devices and are registered in the EUDAQD (eudamed) database. The manufacturer is based in Sweden.
Catalogue
Arm table Ref 10030-01
Regimes: CE MDR Registry: EUDAMED
Company details
- EUDAMED SRN
- SE-MF-000003281
- FDA FEI number
- 3013300766
- EU VAT number
- SE556392736601
- EUDAMED status
- Active
- EUDAMED registered name
- Remeda AB
- Registered address
- 8, Transportvägen, 30230, Halmstad, Sweden
- Website
- www.remeda.com
- linkedin.com/company/remeda-ab
- facebook.com/remedasweden
- [email protected]
- Phone
- +4635158470
- PRRC contact
- Joel Svensson
From the company website
Remeda is a medical technology company with ergonomics in focus. Our products are developed to help reduce strain found in the hospital.
Frequently asked questions
How many devices does Remeda AB have in the registry?
The registry currently lists 1 device for Remeda AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Remeda AB's devices?
Among its 1 most recently registered device, Remeda AB has devices listed in EUDAMED (1 device).
What risk classes do Remeda AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Remeda AB's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Remeda AB in the registry?
The most recently registered devices listed for Remeda AB include Arm table.