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Bicontact E

by Aesculap AG 17 variants

Ref NT1078R, NT1068R, NT1031R, NT1062R, NT1070R, NT1035R, NT1026, NT1020R, NT1050R, NT1083R, NT1018R, NT1051R, NT1024R, NT1009R, NT1063R, NT1087R, NT1014R, NT1090R, NT1011R, NT1039R, NT1079R, NT1025R, NT1040R, NT1056R, NT1069R, NT1003R, NT1001R, NT1015R, NT1008R, NT1000, NT1028R, NT1034R, NT1059R, NT1067R, NT1030R, NT1049R, NT1029R, NT1013R

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 Number40392390000019463B Basic UDI-DI Date25 Nov 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  • Withdrawn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
BICONTACT instrument IIa
BICONTACT instrument Ir
BICONTACT instrument set Ir
BICONTACT tray
BICONTACT instrument set IIa
Model / Reference
NT1078R, NT1068R, NT1031R, NT1062R, NT1070R, NT1035R, NT1026, NT1020R, NT1050R, NT1083R, NT1018R, NT1051R, NT1024R, NT1009R, NT1063R, NT1087R, NT1014R, NT1090R, NT1011R, NT1039R, NT1079R, NT1025R, NT1040R, NT1056R, NT1069R, NT1003R, NT1001R, NT1015R, NT1008R, NT1000, NT1028R, NT1034R, NT1059R, NT1067R, NT1030R, NT1049R, NT1029R, NT1013R
Primary DI / UDI-DI
04046964278532, 04046964278501, 04046964278303, 04046964278440, 04046964278525, 04046964278341, 04046964502064, 04046964278259, 04046964787690, 04046964278587, 04046964278235, 04046964787805, 04046964278266, 04046964278143, 04046964278457, 04046964278709, 04046964278198, 04046964278730, 04046964278167, 04046964278389, 04046964278549, 04046964468568, 04046964278396, 04046964787850, 04046964278518, 04046964501975, 04046964501951, 04046964278204, 04046964278136, 04046964501944, 04046964278273, 04046964278334, 04046964278419, 04046964278495, 04046964277696, 04046964787683, 04046964278280, 04046964278181
Basic UDI-DI
40392390000019463B, 40392390000004542A, 4039239000000310ZE, 4039239000000314ZN, 40392390000019473D
Direct Marketing DI
04046964278532
04046964278501
04046964278303
04046964278440
04046964278525
04046964278341
04046964278259
04046964787690
04046964278587
04046964278235
04046964787805
04046964278266
04046964278143
04046964278457
04046964278709
04046964278198
04046964278730
04046964278167
04046964278389
04046964278549
04046964468568
04046964278396
04046964787850
04046964278518
04046964501975
04046964501951
04046964278204
04046964278136
04046964278273
04046964278334
04046964278419
04046964278495
04046964277696
04046964787683
04046964278280
04046964278181
EMDN Code
L091199, S010401
Device Class
Class IIa
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Reusable NoEUDAMEDYesEUDAMED
  • CMR Substance YesEUDAMEDNoEUDAMED

Other properties (11)

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