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Turon MedTech AB

Sweden Last updated 25 Oct 2026

Devices
16
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue16

  • Ga 20 Ref 020504

    Class I EUDAMED Active

  • Ga 18 Open Ref 020511

    Class I EUDAMED Active

  • Ga 20 Open Ref 020505

    Class I EUDAMED Active

  • Ga 16 Ref 020502

    Class I EUDAMED Active

  • Ga 20 Ref 020302

    Class I EUDAMED Active

  • Ga 12 Ref 020312

    Class I EUDAMED Active

  • Ga 12 Ref 020509

    Class I EUDAMED Active

  • Ga 22 Ref 020311

    Class I EUDAMED Active

  • Ga 22 Ref 020510

    Class I EUDAMED Active

  • Ga 18 Ref 020503

    Class I EUDAMED Active

  • Ga 14 Ref 020307

    Class I EUDAMED Active

  • Ga 13 Ref 020508

    Class I EUDAMED Active

  • Ga 16 Ref 020308

    Class I EUDAMED Active

  • Ga 20 Open Ref 020309

    Class I EUDAMED Active

  • Ga 18 Ref 020301

    Class I EUDAMED Active

  • Ga 14 Ref 020501

    Class I EUDAMED Active

EUDAMED certificates1

EUDAMED certificates (1)

Intertek Medical Notified Body AB 2862 1 certificate

  • 28620168400 Issued

    Quality assurance EU MDR

    Issued
    26 Feb 2024
    Expires
    29 Oct 2028

Related companies

What Turon MedTech AB makes

Turon MedTech AB manufactures single-use, open-ended guidewires labeled with varying gauge sizes (Ga 12 to Ga 22), designed for vascular access procedures. These devices are intended for use in interventional radiology and cardiology to facilitate catheter insertion or navigation within blood vessels.

The company’s guidewires are classified as Class I medical devices under EU regulations and are registered in the EUDAQD database (eudamed). The portfolio is listed under the EU Medical Device Regulation (MDR) framework, with the company headquartered in Sweden.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

How many devices does Turon MedTech AB have in the registry?

The registry currently lists 16 devices for Turon MedTech AB. Devices recorded under merged duplicate company entries are counted once.

Which registries list Turon MedTech AB's devices?

Among its 16 most recently registered devices, Turon MedTech AB has devices listed in EUDAMED (16 devices).

What risk classes do Turon MedTech AB's devices fall under?

Among its 16 most recently registered devices, the classes recorded for Turon MedTech AB's devices are Class I. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Turon MedTech AB?

EUDAMED lists 1 certificate for Turon MedTech AB (quality assurance) under MDR. 1 is recorded with the status issued. The most recent was issued on 2024-02-26.

What are the newest devices from Turon MedTech AB in the registry?

The most recently registered devices listed for Turon MedTech AB include Ga 20, Ga 18 Open, Ga 20 Open and Ga 16.

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

Information

Address
21, Kardanvägen, Varberg, Sweden
Phone
034084060
PRRC contact
Per Englesson
EUDAMED SRN
SE-MF-000033162
FDA FEI number
3007335051