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Iq Columbus Ucr

by Aesculap AG 16 variants

Ref NQ1231, NQ1291R, NQ1220, NQ1232, NQ1215, NQ1004, NQ1202, NQ1294R, NQ1273R, NQ1293R, NQ1275R, NQ1204, NQ1230, NQ1211, NQ1026, NQ1243, NQ1002, NQ1241, NQ1253, NQ1244, NQ1223, NQ1240, NQ1009, NQ1073R, NQ1210, NQ1024, NQ1205, NQ1242, NQ1213, NQ1295R, NQ1221, NQ1037R, NQ1203, NQ1212, NQ1001, NQ1027, NQ1222, NQ1255, NQ1252

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 Number40392390000016422L 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  • Withdrawn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

Trade Name
Iq Columbus Ucr
Iq Columbus
Device Name
COLUMBUS implantation instrument IIa
COLUMBUS instrument set
COLUMBUS implantation instrument Ir
COLUMBUS instrument tray
Model / Reference
NQ1231, NQ1291R, NQ1220, NQ1232, NQ1215, NQ1004, NQ1202, NQ1294R, NQ1273R, NQ1293R, NQ1275R, NQ1204, NQ1230, NQ1211, NQ1026, NQ1243, NQ1002, NQ1241, NQ1253, NQ1244, NQ1223, NQ1240, NQ1009, NQ1073R, NQ1210, NQ1024, NQ1205, NQ1242, NQ1213, NQ1295R, NQ1221, NQ1037R, NQ1203, NQ1212, NQ1001, NQ1027, NQ1222, NQ1255, NQ1252
Primary DI / UDI-DI
04046964157219, 04046964173066, 04046964156984, 04046964157936, 04046964157981, 04046964218309, 04046964158124, 04046964173097, 04046964247675, 04046964173080, 04046964247699, 04046964158100, 04046964157202, 04046964157875, 04046964229190, 04046964157837, 04046964218286, 04046964157233, 04046964157745, 04046964157820, 04046964157967, 04046964157226, 04046964217739, 04046964800047, 04046964157882, 04046964218316, 04046964157899, 04046964157844, 04046964158001, 04046964173103, 04046964156991, 04046964370977, 04046964158117, 04046964158018, 04046964218279, 04046964370960, 04046964157974, 04046964157721, 04046964157752
Basic UDI-DI
40392390000016422L, 403923900000256634, 4039239000000331ZN, 4039239000000330ZL
Direct Marketing DI
04046964173066
04046964173097
04046964247675
04046964173080
04046964247699
04046964800047
04046964173103
04046964370977
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

Other properties (12)

  • Sterile: No
  • Implantable: 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