Bohus BioTech AB
Active in EUDAMEDSwedenfrom SRN EUDAMED SRN SE-MF-000037369
- Devices
- 37
- Registrations
- EUDAMED
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
What Bohus BioTech AB makes
Bohus BioTech AB manufactures hyaluronic acid-based products for ophthalmic, aesthetic, and orthopaedic applications, including injectable fillers (e.g., DERMHAGE FINE TOUCH, DERMHAGE VOLUME, Elevate Ultra), intraocular viscosurgical devices (e.g., ViscoVita), and orthopaedic joint supplements (e.g., chondrovital). The portfolio also includes dermal and soft tissue enhancement systems (e.g., DECORIA, TULISMA) and specialized ophthalmic lines (e.g., INTRALINE).
The company’s products are classified under EU Medical Device Regulations as Class III (e.g., ophthalmic viscosurgical devices) and Class IIb (e.g., aesthetic and orthopaedic hyaluronic acid products), with all devices listed in the EU’s eudamed registry. Bohus BioTech AB is headquartered in Sweden.
Catalogue
Search and filter all 37 devicesCompany details
- EUDAMED SRN
- SE-MF-000037369
- EU VAT number
- SE5565000709
- EUDAMED status
- Active
- EUDAMED registered name
- Bohus BioTech AB
- EUDAMED abbreviated name
- BOHUS
- Registered address
- 4, Trädgårdsgatan, 45231, Strömstad, Sweden
- Website
- www.bohusbiotech.com
- [email protected]
- Phone
- +46 526 14686
- PRRC contact
- Mehrdad Jalali
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 30 Mar 2031
Notified body 2797 1 certificate
- MDR 792676 Active
Quality management system EU MDR
- Issued
- 15 Jun 2026
- Expires
- 30 Mar 2031
- Reason
- Add device or group
Frequently asked questions
How many devices does Bohus BioTech AB have in the registry?
The registry currently lists 37 devices for Bohus BioTech AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bohus BioTech AB's devices?
Among its 37 most recently registered devices, Bohus BioTech AB has devices listed in EUDAMED (37 devices).
What risk classes do Bohus BioTech AB's devices fall under?
Among its 37 most recently registered devices, the classes recorded for Bohus BioTech AB's devices are Class IIb and Class III. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Bohus BioTech AB?
EUDAMED lists 1 certificate for Bohus BioTech AB (quality management system) under MDR. The most recent was issued on 2026-06-15.
What are the newest devices from Bohus BioTech AB in the registry?
The most recently registered devices listed for Bohus BioTech AB include DECORIA Pure Lips, Dermafill Global Xtra, SweDermis Lift and Dermafill Lips.