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Lomba-Go

by Thuasne Deutschland GmbH 22 variants

Ref T30145620101199, T30145320101199, T35145620401199, T35145220101199, T35140620101199, T30145620301199, T35145620301199, T30145320601199, T30145620501199, T35140220501199, T35145620501199, T35140220201199, T35145220501199, T30140320201199, T35145620201199, T35145620101199, T30140420301699, T35145220401199, T30140320601199, T35140620501199, T30145620601199, T35140620401199, T35140220401199, T30145320501199, T35140220101199, T30140320501199, T30140320301199, T30145320201199, T35140620601199, T30140620101199, T35140220301199, T35140620201199

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4035459DE0501B3D Basic UDI-DI Date8 Dec 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Lomba-Go
Model / Reference
T30145620101199, T30145320101199, T35145620401199, T35145220101199, T35140620101199, T30145620301199, T35145620301199, T30145320601199, T30145620501199, T35140220501199, T35145620501199, T35140220201199, T35145220501199, T30140320201199, T35145620201199, T35145620101199, T30140420301699, T35145220401199, T30140320601199, T35140620501199, T30145620601199, T35140620401199, T35140220401199, T30145320501199, T35140220101199, T30140320501199, T30140320301199, T30145320201199, T35140620601199, T30140620101199, T35140220301199, T35140620201199
Primary DI / UDI-DI
04035459286541, 04035459328654, 04035459320801, 04035459320719, 04035459320658, 04035459286565, 04035459320795, 04035459328708, 04035459286589, 04035459320634, 04035459320818, 04035459320603, 04035459320757, 04035459328593, 04035459320788, 04035459320771, 04035459424295, 04035459320740, 04035459328630, 04035459320696, 04035459286596, 04035459320689, 04035459320627, 04035459328692, 04035459320597, 04035459328623, 04035459328609, 04035459328661, 04035459320702, 04035459286428, 04035459320610, 04035459320665
Basic UDI-DI
4035459DE0501B3D, 4035459DE0501A3B
Direct Marketing DI
04035459286541
04035459328654
04035459320801
04035459320719
04035459320658
04035459286565
04035459320795
04035459328708
04035459286589
04035459320634
04035459320818
04035459320603
04035459320757
04035459328593
04035459320788
04035459320771
04035459424295
04035459320740
04035459328630
04035459320696
04035459286596
04035459320689
04035459320627
04035459328692
04035459320597
04035459328623
04035459328609
04035459328661
04035459320702
04035459286428
04035459320610
04035459320665
EMDN Code
Y060309 Thoracolumbosacral spine orthoses
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
DE-MF-000006210

Other devices from Thuasne Deutschland GmbH

See all devices from Thuasne Deutschland GmbH →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No