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Dassiet Oy

Finland FI-MF-000016466 Last updated 30 May 2026

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Devices
75
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue75

Page 1 of 2

  • Ucast Ref U-THUMB

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref U-ANKLE

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref C1480S Black

    Class I EUDAMED Active

  • Woodcast Ref B1240S

    Class I EUDAMED Active

  • Woodcast Ref C1480S

    Class I EUDAMED Active

  • Procast Ref X0400

    Class I EUDAMED Active

  • Procast Ref X2522

    Class I EUDAMED Active

  • Woodcast Ref B1565

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref TCC8080

    Class I EUDAMED Active

  • Ucast Ref U-HUM-L

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref A-ANKLE

    Class I EUDAMED Active

  • Ucast Ref U-MC

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref U-THUMB-SH

    Class I EUDAMEDFDA UDI Active

  • Procast Ref X7522

    Class I EUDAMED Active

  • Woodcast Ref C1465pm

    Class I EUDAMED Active

  • Woodcast Ref F1480S

    Class I EUDAMED Active

  • Woodcast Ref C1465 Black

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref B1280

    Class I EUDAMED Active

  • Woodcast Ref B1580

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref B1565 Black

    Class I EUDAMEDFDA UDI Active

  • Procast Ref X5251

    Class I EUDAMED Active

  • Procast Ref X4350

    Class I EUDAMED Active

  • Ucast Ref A-KNEE

    Class I EUDAMED Active

  • Woodcast Ref B1040

    Class I EUDAMED Active

  • Ucast Ref A-WRIST-L

    Class I EUDAMED Active

  • Procast Ref A002

    Class I EUDAMED Active

  • Woodcast Ref C1480 Black

    Class I EUDAMED Active

  • Ucast Ref A-THUMB-SH

    Class I EUDAMED Active

  • Woodcast Ref B1580 Black

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref C1441 Black

    Class I EUDAMEDFDA UDI Active

  • Procast Ref X5252

    Class I EUDAMED Active

  • Woodcast Ref C1441

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref C1434S

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref C1434 Black

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref C1480S Blue

    Class I EUDAMED Active

  • Ucast Ref A-THUMB-R

    Class I EUDAMED Active

  • Woodcast Ref F1480

    Class I EUDAMED Active

  • Ucast Ref U-MALLET

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref A-WRIST-R

    Class I EUDAMED Active

  • Woodcast Ref F1434

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref U-KNEECAP

    Class I EUDAMEDFDA UDI Active

  • Procast Ref X5250

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref A-HEEL

    Class I EUDAMED Active

  • Procast Ref X4350A

    Class I EUDAMEDFDA UDI Active

  • Woodcast Ref B1080

    Class I EUDAMED Active

  • Woodcast Ref C1434S Black

    Class I EUDAMEDFDA UDI Active

  • Uno Ref U-EMS3

    Class I EUDAMEDFDA UDI Active

  • Ucast Ref U-FINGER-LONG

    Class I EUDAMEDFDA UDI Active

  • Procast Ref X1022

    Class I EUDAMED Active

  • Uno Ref U-TACT3

    Class I EUDAMEDFDA UDI Active

Showing 1-50 of 75

What Dassiet Oy makes

Dassiet Oy manufactures sterile cotton wool rolls, including variants branded as UCAST, WOODCAST, and PROCAST, designed for medical and clinical use.

These products fall under EU Medical Device Regulation as Class I devices and are registered in the EUDAQS database via eudamed.

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

Frequently asked questions

What types of medical devices does Dassiet Oy manufacture?

Dassiet Oy specializes in sterile cotton wool rolls, which are essential for medical and clinical applications. Their product line includes variants branded as UCAST, WOODCAST, and PROCAST, all serving as disposable swabs or dressings for wound care, cleaning, or diagnostic procedures.

Where is Dassiet Oy based?

Dassiet Oy is headquartered in Finland, operating as a Finnish manufacturer of medical devices. Their location influences regulatory compliance with EU standards, particularly for devices marketed within the European Economic Area.

Which regulatory registries list Dassiet Oy’s devices?

Dassiet Oy’s devices are listed in the EUDAQS database under eudamed, the official EU portal for medical device information. This registry is required for Class I devices under the EU Medical Device Regulation (MDR) to ensure traceability and compliance.

How are Dassiet Oy’s devices classified under EU regulations?

All of Dassiet Oy’s listed devices fall under Class I classification in the EU Medical Device Regulation. This classification applies to low-risk products like sterile cotton wool rolls, which pose minimal risk to patients and users, requiring basic conformity assessment procedures.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Finland
Address
14, Tekniikantie, Espoo, Finland
Phone
+358504664642
PRRC contact
Eija Pirhonen
EUDAMED SRN
FI-MF-000016466
DUNS number
651254398