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WUNDER SA.BI. S.R.L.

Italy Last updated 17 Sep 2026

Devices
71
Registries
EUDAMED
FDA recalls
0

Catalogue71

Page 2 of 2

  • R150A Ref 00021A

    Class I EUDAMED Active

  • Rw-Xl Ref 00092T

    Class I EUDAMED Active

  • Rw-Xl Ref 00092TA

    Class I EUDAMED Active

  • RA con WH200D Ref 00071A+00051D

    Class I EUDAMED Active

  • Ps-20 Ref 00090G

    Class I EUDAMED Active

  • Rl Ref 00094B

    Class I EUDAMED Active

  • Rw 2.0 Move Ref 00092R

    Class I EUDAMED Active

  • Rb-Cavo Ref 00071N

    Class I EUDAMED Active

  • BABY02 con WH80D Ref 000482IA+00060HM

    Class I EUDAMED Active

  • RW02 Ref 00092D

    Class I EUDAMED Active

  • RW3.0 Ref 00092M

    Class I EUDAMED Active

  • Rb Ref 00071I

    Class I EUDAMED Active

  • Pl-Vega Ref EBT510W

    Class I EUDAMED Active

  • RW02 Ref 00092I

    Class I EUDAMED Active

  • BABY02 con WH80D Ref 000482C+00060HM

    Class I EUDAMED Active

  • C202 Ref 00008C

    Class I EUDAMED Active

  • BABY02 con WH80D Ref 000482E+00060HM

    Class I EUDAMED Active

  • RS300 Ref 00090E

    Class I EUDAMED Active

  • BABY02 con WH80 Ref 000482C+00060M

    Class I EUDAMED Active

  • R2020 Ref 73

    Class I EUDAMED Active

  • BABY02 con WH80D Ref 000482G+00060HM

    Class I EUDAMED Active

Showing 51-71 of 71

EUDAMED certificates1

EUDAMED certificates (1)

ICIM S.P.A. 0425 1 certificate

  • 0425-MDR-030050-01 Issued

    Quality assurance EU MDR

    Issued
    29 Oct 2024
    Expires
    22 Oct 2028

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About

For more than fifty years Wunder is inspired by what is not only an idea, but a philosophy that guides our work: precision.

Translated from the manufacturer's own website. Source

What WUNDER SA.BI. S.R.L. makes

Wunder SA.BI. S.R.L. manufactures a range of Class I medical devices primarily focused on respiratory and neonatal care, including ventilators (e.g., RW 2.0 MOVE, PL-VEGA, PS-20), neonatal ventilators (e.g., BABY02 con WH80, SUPERBABY), and respiratory support systems (e.g., RA con WH200D, R2020 con WH200). Additional products include portable respiratory devices (e.g., PL-AP4300) and monitoring or accessory units (e.g., C201, RH, RB con WH200).

The company’s devices are classified under EU Class I and are listed in the EUDAMED registry. Wunder SA.BI. S.R.L. is based in Italy and adheres to EU medical device regulations, ensuring compliance with mandatory requirements for Class I products.

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

Information

Address
7, VIA MONTE GRAPPA, BERGAMO, Italy
Website
www.wunder.it
Phone
+39 02 90964566
PRRC contact
Riccardo Bassi
EUDAMED SRN
IT-MF-000028482