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Challenger® Ti

by Aesculap AG 2 variants

Ref PL572T

Active European Union

CE MDR

Valid until

7 Oct 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number20201GB450260922 Date22 Sep 2026IssuedStatusActive expires 7 Oct 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20201GB450260922 Active Reissued

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    22 Sep 2026
    Expires
    7 Oct 2031
    Valid from
    8 Oct 2026

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

EU market availability

Made available in 27 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 4 Nov 2002
  • Belgium since 4 Nov 2002
  • Bulgaria since 4 Nov 2002
  • Croatia since 4 Nov 2002
  • Cyprus since 4 Nov 2002
  • Czechia since 4 Nov 2002
  • Denmark since 4 Nov 2002
  • Estonia since 4 Nov 2002
  • Finland since 4 Nov 2002
  • France since 4 Nov 2002
  • Germany since 4 Nov 2002
  • Greece since 4 Nov 2002
  • Hungary since 4 Nov 2002
  • Ireland since 4 Nov 2002
  • Italy since 4 Nov 2002
  • Latvia since 4 Nov 2002
  • Lithuania since 4 Nov 2002
  • Luxembourg since 4 Nov 2002
  • Malta since 4 Nov 2002
  • Netherlands since 4 Nov 2002
  • Poland since 4 Nov 2002
  • Portugal since 4 Nov 2002
  • Romania since 4 Nov 2002
  • Slovakia since 4 Nov 2002
  • Slovenia since 4 Nov 2002
  • Spain since 4 Nov 2002
  • Sweden since 4 Nov 2002

Last checked 25 Oct 2026.

Specification

EUDAMED

Device Name
CHALLENGER clip
Model / Reference
PL572T
Primary DI / UDI-DI
04038653341856
Basic UDI-DI
40392390000005772T
EMDN Code
H03020103 Reusable multiple clip appliers for videosurgery
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005504

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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