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Wallaby Medical

Active in EUDAMED
Also registered as Wallaby Medical, Inc.

United Statesfrom SRN EUDAMED FDA SRN US-MF-000010241 FEI 3012543881

Devices
257
Registrations
EUDAMEDFDA
FDA recalls
0

What Wallaby Medical makes

Wallaby Medical manufactures the Wallaby Avenir™ Coil System, a medical device used for vascular embolization procedures.

The Wallaby Avenir™ Coil System is classified as Class II and Class III and is listed in the EUDAMED and FDA 510(k) registries. Wallaby Medical is based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue257

Newest first, rows 251-257 of 257

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  • Wallaby Avenir™ Coil System Ref 10CFN03008

    Active Regimes: CE MDR CE MDD Registry: EUDAMEDGUDID Class:III

  • Wallaby Avenir™ Coil System Ref 10CFR02006

    Active Regimes: CE MDR CE MDD Registry: EUDAMEDGUDID Class:III

  • Wallaby Avenir™ Coil System Ref 10HFN01502

    Active Regimes: CE MDR CE MDD Registry: EUDAMEDGUDID Class:III

  • Wallaby Avenir™ Coil System Ref 10CFN01002

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:III

  • Wallaby Avenir™ Coil System Ref 10HFL08030

    Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:III

  • Wallaby Avenir™ Coil System Ref 10HFL10030

    Active Regimes: CE MDR CE MDD Registry: EUDAMEDGUDID Class:III

  • Wallaby Avenir™ Coil System Ref 10CFN02004

    Active Regimes: CE MDR CE MDD Registry: EUDAMEDGUDID Class:III

Showing 251-257 of 257

Company details

EUDAMED SRN
US-MF-000010241
FDA FEI number
3012543881
EUDAMED status
Active
EUDAMED registered name
Wallaby Medical
Registered address
22901, Mill Creek Drive, 92653, Laguna Hills, United States
Phone
+1 858.437.2286
PRRC contact
Nathaniel Knock(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 22 Jul 2030

EUDAMED certificates (1)

BSI Group The Netherlands B.V. 2797 1 certificate

  • MDR 807342 Active Supplemented

    Technical documentation EU MDR

    Issued
    20 Aug 2026
    Expires
    22 Jul 2030
    Reason
    Change approved