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Plasmafit

by Aesculap AG 16 variants

Ref NT1547, NT534, NT402, NT533, NT1515, NT1544, NT480, NT471R, NT476R, NT478R, NT475R, NT592, NT1571R, NT716, NT1516, NT404, NT472R, NT496, NT1501R, NT532, NT495, NT474R, NT595, NT593, NT436, NT1545, NT426R, NT497, NT498, NT717, NT1543, NT594, NT473R, NT1512, NT481R, NT713, NT1517, NT535, NT715

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40392390000019593L 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  • Withdrawn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
PLASMAFIT instrument IIa
PLASMAFIT instrument set
PLASMAFIT tray
Model / Reference
NT1547, NT534, NT402, NT533, NT1515, NT1544, NT480, NT471R, NT476R, NT478R, NT475R, NT592, NT1571R, NT716, NT1516, NT404, NT472R, NT496, NT1501R, NT532, NT495, NT474R, NT595, NT593, NT436, NT1545, NT426R, NT497, NT498, NT717, NT1543, NT594, NT473R, NT1512, NT481R, NT713, NT1517, NT535, NT715
Primary DI / UDI-DI
04046955350100, 04046964649455, 04046964093494, 04046964649448, 04046955350001, 04046955350070, 04046964098444, 04046964098451, 04046964098505, 04046964098529, 04046964098499, 04046964649479, 04046955582150, 04046955312108, 04046955350018, 04046964093357, 04046964098468, 04046964098550, 04046955351503, 04046964649431, 04046964098543, 04046964098482, 04046964649509, 04046964649486, 04046964093364, 04046955350087, 04046964021022, 04046964098567, 04046964098574, 04046955312115, 04046955350063, 04046964649493, 04046964098475, 04046955349975, 04046964098437, 04046955312078, 04046955350025, 04046964649462, 04046955312092
Basic UDI-DI
40392390000019593L, 40392390000019583J, 40392390000003892Q
Direct Marketing DI
04046964649455
04046964649448
04046955350001
04046964098451
04046964098505
04046964098529
04046964098499
04046964649479
04046955582150
04046955312108
04046955350018
04046964098468
04046964098550
04046955351503
04046964649431
04046964098543
04046964098482
04046964649509
04046964649486
04046964098567
04046964098574
04046955312115
04046964649493
04046964098475
04046955349975
04046964098437
04046955312078
04046964649462
04046955312092
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

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