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Spex Ltd

New Zealand Last updated 25 Oct 2026

Devices
12,047
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue12,047

Page 20 of 40

  • Spex Ref 1106-1618-0SS_044

    Class I EUDAMED Active

  • Spex Ref 1254-1420-000-C_054

    Class I EUDAMED Active

  • Spex Ref 1103-2424-0SC_054

    Class I EUDAMED Active

  • Spex Ref 1254-1214-200-C_060

    Class I EUDAMED Active

  • Spex Ref 1254-1418-000

    Class I EUDAMED Active

  • Spex Ref 1254-1316-000-S

    Class I EUDAMED Active

  • Spex Ref 1252-1618-4HA-C_060

    Class I EUDAMED Active

  • Spex Ref 1136-1414-7HC_090

    Class I EUDAMED Active

  • Spex Ref 1256-1012-0SS-C

    Class I EUDAMED Active

  • Spex Ref 1255-1718-0SS-C_028

    Class I EUDAMED Active

  • Spex Ref 1254-1012-000_090

    Class I EUDAMED Active

  • Spex Ref 1255-1412-0TS

    Class I EUDAMED Active

  • Spex Ref 1257-1822-30K-FC

    Class I EUDAMED Active

  • Spex Ref 1258-2620-0SS_054

    Class I EUDAMED Active

  • Spex Ref 1255-1614-0TS-C_044

    Class I EUDAMED Active

  • Spex Ref 1123-20XX-6SC_090

    Class I EUDAMED Active

  • Spex Ref 1255-1618-0TS-F

    Class I EUDAMED Active

  • Spex Ref 1257-2020-30K-C_044

    Class I EUDAMED Active

  • Spex Ref 1251-1415-0AM-FC

    Class I EUDAMED Active

  • Spex Ref 1103-18XX-0SC

    Class I EUDAMED Active

  • Spex Ref 1257-1618-3FK-C_044

    Class I EUDAMED Active

  • Spex Ref 1123-13XX-6HC_028

    Class I EUDAMED Active

  • Spex Ref 1255-1520-0TS_060

    Class I EUDAMED Active

  • Spex Ref 1113-07-1414

    Class I EUDAMED Active

  • Spex Ref 1254-1518-000-C_044

    Class I EUDAMED Active

  • Spex Ref 1255-18XX-0TS_060

    Class I EUDAMED Active

  • Spex Ref 1255-1614-0GA_209

    Class I EUDAMED Active

  • Spex Ref 1256-1614-0SS-C_090

    Class I EUDAMED Active

  • Spex Ref 1258-2929-00H-C_022

    Class I EUDAMED Active

  • Spex Ref 1136-1414-7SS_077

    Class I EUDAMED Active

  • Spex Ref 1126-1516-6HC_090

    Class I EUDAMED Active

  • Spex Ref 1258-2216-0SS_030

    Class I EUDAMED Active

  • Spex Ref 1156-0203-000

    Class I EUDAMED Active

  • Spex Ref 1252-1817-00M-C_054

    Class I EUDAMED Active

  • Spex Ref 1255-1318-0SS-S

    Class I EUDAMED Active

  • Spex Ref 1255-1716-0TS-C_090

    Class I EUDAMED Active

  • Spex Ref 1252-1414-00M-C_028

    Class I EUDAMED Active

  • Spex Ref 1252-1112-00H-S

    Class I EUDAMED Active

  • Spex Ref 1126-1718-6SC_028

    Class I EUDAMED Active

  • Spex Ref 1252-1520-00H_044

    Class I EUDAMED Active

  • Spex Ref 1106-1518-0SC_030

    Class I EUDAMED Active

  • Spex Ref 1255-1816-0TS-C_030

    Class I EUDAMED Active

  • Spex Ref 1105-1818-0SS_077

    Class I EUDAMED Active

  • Spex Ref 1126-1718-6HC_044

    Class I EUDAMED Active

  • Spex Ref 1257-2020-003-FC_090

    Class I EUDAMED Active

  • Spex Ref 1255-2929-0SS-F

    Class I EUDAMED Active

  • Spex Ref 1123-17XX-6SC_054

    Class I EUDAMED Active

  • Spex Ref 1255-11XX-0SS-FC_077

    Class I EUDAMED Active

  • Spex Ref 1255-1923-0SS-I

    Class I EUDAMED Active

  • Spex Ref 1106-1516-0HC_054

    Class I EUDAMED Active

Showing 951-1,000 of 12,047

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Authorised representatives

What Spex Ltd makes

Spex Ltd manufactures a range of Class I medical devices, including the Lateral Trunk Support and the Spex Wonderseat, which are designed for patient positioning and support in clinical settings. Additional products include multiple iterations of the Spex device, as well as the Spex for Bingo, which appears tailored for specific patient care applications.

The company’s portfolio is regulated under Class I medical devices in the EU, with devices listed in the EUDAMED database. Spex Ltd is based in New Zealand and adheres to relevant regulatory requirements for these products.

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

Information

Address
1, Pereita Drive, Rolleston, New Zealand
Phone
006433079790
PRRC contact
Michael Vent
EUDAMED SRN
NZ-MF-000009327
FDA FEI number
3012958676