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Spex Ltd

New Zealand Last updated 25 Oct 2026

Devices
12,047
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue12,047

Page 26 of 40

  • Spex Ref 1123-1718-6HC_044

    Class I EUDAMED Active

  • Spex Ref 1125-1212-6HC_054

    Class I EUDAMED Active

  • Spex Ref 1106-1620-0SS_030

    Class I EUDAMED Active

  • Spex Ref 1255-1618-TGA_209

    Class I EUDAMED Active

  • Spex Ref 1123-1718-6SC

    Class I EUDAMED Active

  • Spex Ref 1257-2020-3FK_044

    Class I EUDAMED Active

  • Spex Ref 1257-1824-003-FC_044

    Class I EUDAMED Active

  • Spex Ref 1257-1618-3F0-FC_090

    Class I EUDAMED Active

  • Spex Ref 1136-1720-7SC_054

    Class I EUDAMED Active

  • Spex Ref 1103-18XX-0HC_054

    Class I EUDAMED Active

  • Spex Ref 1105-2418-0SS_077

    Class I EUDAMED Active

  • Spex Ref 1126-1720-6HC_022

    Class I EUDAMED Active

  • Spex Ref 1254-1720-200_028

    Class I EUDAMED Active

  • Spex Ref 1255-1518-0TS-I

    Class I EUDAMED Active

  • Spex Ref 1123-2424-6SC

    Class I EUDAMED Active

  • Spex Ref 1255-1014-0SS-FICB

    Class I EUDAMED Active

  • Spex Ref 1123-1618-6SC_090

    Class I EUDAMED Active

  • Spex Ref 1123-17XX-6SC_044

    Class I EUDAMED Active

  • Spex Ref 1255-11XX-0TS-C_030

    Class I EUDAMED Active

  • Spex Ref 1257-2939-300-C_077

    Class I EUDAMED Active

  • Spex Ref 1125-11XX-6HC_030

    Class I EUDAMED Active

  • Spex Ref 1105-2422-0SC

    Class I EUDAMED Active

  • Spex Ref 1257-1418-300-FC

    Class I EUDAMED Active

  • Spex Ref 1103-11XX-0HC_077

    Class I EUDAMED Active

  • Spex Ref 1123-2422-6HC_060

    Class I EUDAMED Active

  • Spex Ref 1105-1822-0SS_090

    Class I EUDAMED Active

  • Spex Ref 1106-1720-0SC_090

    Class I EUDAMED Active

  • Spex Ref 1255-1823-0TS-S

    Class I EUDAMED Active

  • Spex Ref 1257-1820-30K-C

    Class I EUDAMED Active

  • Spex Ref 1255-15XX-0SS-FC_044

    Class I EUDAMED Active

  • Spex Ref 1105-2218-0SS_044

    Class I EUDAMED Active

  • Spex Ref 1136-1618-7SS_060

    Class I EUDAMED Active

  • Spex Ref 1123-2022-6HC_044

    Class I EUDAMED Active

  • Spex Ref 1255-1416-0SS-FC_060

    Class I EUDAMED Active

  • Spex Ref 1254-1418-200_060

    Class I EUDAMED Active

  • Spex Ref 1123-2020-6HC_044

    Class I EUDAMED Active

  • Spex Ref 1254-1014-000_077

    Class I EUDAMED Active

  • Spex Ref 1257-1418-3FK-FC

    Class I EUDAMED Active

  • Spex Ref 1126-1620-6SC_044

    Class I EUDAMED Active

  • Spex Ref 1123-11XX-6SC_028

    Class I EUDAMED Active

  • Spex Ref 1136-1620-7SC_054

    Class I EUDAMED Active

  • Spex Ref 1255-1816-0SS-C_044

    Class I EUDAMED Active

  • Spex Ref 1256-1618-0SS-C_022

    Class I EUDAMED Active

  • Spex Ref 1258-2425-200-FC

    Class I EUDAMED Active

  • Spex Ref 1103-1418-0SC_090

    Class I EUDAMED Active

  • Spex Ref 1255-1314-0TS-C_022

    Class I EUDAMED Active

  • Spex Ref 1105-1212-0SH_044

    Class I EUDAMED Active

  • Spex Ref 1103-20XX-0SC_090

    Class I EUDAMED Active

  • Spex Ref 1103-2218-0HC_077

    Class I EUDAMED Active

  • Spex Ref 1125-10XX-6HC_030

    Class I EUDAMED Active

Showing 1,251-1,300 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