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Absorba

by Imtegra GmbH & Co KG 30 variants

Ref 2206 3114, 3203, 2206 9113, 2206 3211, 4205, 2206 3209, 4107, 2102, 9313, 9205, 3115, 2206 3215, 9312, 3207, 2206 3212, 2206 3210, 2206 3201, 2206 3108, 3108, 2206 3101, 4202, 2206 3208, 2206 3105, 2101, 3212, 2206 4107, 4105, 3209, 2206 4201, 3112, 3201, 3114, 3202, 9114, 2206 3206, 9112, 3214, 3110, 2206 9314, 2206 3207, 3107, 2206 4205, 3105, 2206 9312, 2206 9114, 4201, 4101, 4207, 2206 9313, 2206 3107, 3205

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 Number4260253262206S9 Basic UDI-DI Date17 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  • Withdrawn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
Abdecktuch
Abdecktücher
Model / Reference
2206 3114, 3203, 2206 9113, 2206 3211, 4205, 2206 3209, 4107, 2102, 9313, 9205, 3115, 2206 3215, 9312, 3207, 2206 3212, 2206 3210, 2206 3201, 2206 3108, 3108, 2206 3101, 4202, 2206 3208, 2206 3105, 2101, 3212, 2206 4107, 4105, 3209, 2206 4201, 3112, 3201, 3114, 3202, 9114, 2206 3206, 9112, 3214, 3110, 2206 9314, 2206 3207, 3107, 2206 4205, 3105, 2206 9312, 2206 9114, 4201, 4101, 4207, 2206 9313, 2206 3107, 3205
Primary DI / UDI-DI
04260530120395, 04260679314709, 04260368358410, 04260530120531, 04260679314877, 04260530120494, 04260679314846, 04260679314495, 04260679315072, 04262472164819, 04260679314679, 04260530120616, 04260679315065, 04260679314723, 04260530120555, 04260530120517, 04260530120418, 04260530120074, 04260679314624, 04260368355907, 04260679314860, 04260530120470, 04260679312354, 04260679314488, 04260679314778, 04260368356539, 04260679314839, 04260679314747, 04260368355297, 04260679314655, 04260679314686, 04260679314662, 04260679314693, 04260679315003, 04260679313528, 04260679314983, 04260679314792, 04260679314648, 04260530120715, 04260530120456, 04260679314617, 04260368355235, 04260679314600, 04260530120678, 04260368358434, 04260679314853, 04260679314815, 04260679314884, 04260530120692, 04260368355945, 04260679314716
Basic UDI-DI
4260253262206S9, 4260253262206nsGH
EMDN Code
T020199 Surgical drapes - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006451

Other devices from Imtegra GmbH & Co KG

See all devices from Imtegra GmbH & Co KG →

Properties

  • Sterile YesEUDAMEDNoEUDAMED

Other properties (12)

  • 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