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Bohus BioTech AB

Active in EUDAMED

Swedenfrom SRN EUDAMED SRN SE-MF-000037369

Devices
37
Registrations
EUDAMED

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

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.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue37

Newest first, rows 1-37 of 37

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  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Minivisc® Disp Ref Minivisc Disp

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Minivisc® Base Ref Minivisc Base

    Active Regimes: CE MDR Registry: EUDAMED Class:IIb
  • Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • None Regimes: CE, no status data Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Intraline

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • ViscoVita

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Decoria

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Tulisma

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Tulisma

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • chondrovital

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Elevate kiss

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • ViscoPlus

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Minivisc

    Active Regimes: CE MDR CE MDD Registry: EUDAMED Class:IIb
  • Intraline

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Synotec

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • ViscoVita

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Cartinorm

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Tulisma

    Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Active Regimes: CE MDD Registry: EUDAMED Class:III
  • Chondrovital

    Active Regimes: CE MDD Registry: EUDAMED Class:III

Rows 1-37 of 37

Company 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
Phone
+46 526 14686(from company website)
PRRC contact
Mehrdad Jalali(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 30 Mar 2031

EUDAMED certificates (1)

Notified body 2797 1 certificate

  • MDR 792676 Active Supplemented

    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.

Generated automatically from registry data and not verified by a human reviewer.