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Individo-Set

by Imtegra GmbH & Co KG 210 variants

Ref 1014 8010, 1014 7124, 1014 6863, 1014 7043, 1014 7079, 1014 7131, 1014 6296, 1014 6999, 1014 7083, 1014 6650, 1014 6687, 1014 6850, 1014 5710, 1014 6928, 1014 7262, 1014 7428, 1014 6851, 1014 5597, 1014 7130, 1014 2153, 1014 6829, 1014 6747, 1014 6962, 1014 6994, 1014 7104, 1014 7033, 1014 7042, 1014 6872, 1014 6938, 1014 8015, 1014 6898, 1014 7085, 1014 7342, 1014 7208, 1014 6817, 1014 6626, 1014 7189, 1014 6891, 1014 6580, 1014 6964, 1015 5010, 1014 6860, 1014 6940, 1014 7069, 1014 7409, 1014 7049, 1014 7316, 1014 7296, 1014 7354, 1014 6939, 1014 6969

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 linked in EUDAMED

A group certificate may exist

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 Number4260253261014RP Basic UDI-DI Date24 Jan 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Individo-Set - I
Individo-Set - IIa
Model / Reference
1014 8010, 1014 7124, 1014 6863, 1014 7043, 1014 7079, 1014 7131, 1014 6296, 1014 6999, 1014 7083, 1014 6650, 1014 6687, 1014 6850, 1014 5710, 1014 6928, 1014 7262, 1014 7428, 1014 6851, 1014 5597, 1014 7130, 1014 2153, 1014 6829, 1014 6747, 1014 6962, 1014 6994, 1014 7104, 1014 7033, 1014 7042, 1014 6872, 1014 6938, 1014 8015, 1014 6898, 1014 7085, 1014 7342, 1014 7208, 1014 6817, 1014 6626, 1014 7189, 1014 6891, 1014 6580, 1014 6964, 1015 5010, 1014 6860, 1014 6940, 1014 7069, 1014 7409, 1014 7049, 1014 7316, 1014 7296, 1014 7354, 1014 6939, 1014 6969
Primary DI / UDI-DI
04260530122221, 04262472160323, 04260679315546, 04260679318868, 04260679319261, 04262472160590, 04260368358878, 04260679318127, 04260679319469, 04260530128964, 04260530129596, 04260679315249, 04260253268039, 04260679316796, 04262472163027, 04262472165779, 04260679315263, 04260368350407, 04262472160149, 04260530125772, 04260679313832, 04260679311593, 04260679317434, 04260679317922, 04260679319889, 04260679319124, 04260679318523, 04260679315744, 04260679317052, 04260530122207, 04260679316468, 04260679319360, 04262472165595, 04262472161962, 04260679313504, 04260530128421, 04262472161672, 04260679316222, 04260530127646, 04260679317519, 04260679313412, 04260679315492, 04260679317090, 04260679319087, 04262472165533, 04260679318608, 04262472164062, 04262472163522, 04262472164222, 04260679317014, 04260679317557
Basic UDI-DI
4260253261014RP, 4260253261001RE
EMDN Code
V0599 Clinical procedures kits not included in other classes - other
Device Class
Class I
Class IIa
Medical Purpose
zur Unterstützung einer medizinischen Behandlung

Manufacturer details

EUDAMED SRN
DE-PR-000006448

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Properties

  • Sterile