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aerstent TBS

by bess pro gmbh Germany EUDAMED

Ref 503-16-060

EMDN P0401

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4063106ASTAERLX Basic UDI-DIDate7 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 1000310118 Issued

    Technical documentation EU MDR

    Notified body
    Notified body 0297
    Issued
    2 Jul 2026
    Expires
    1 Jul 2031
  • 1000301888 Supplemented

    Quality management system EU MDR

    Notified body
    Notified body 0297
    Issued
    2 Jul 2026
    Expires
    27 Feb 2030
    Reason
    Change approved

Specification

EUDAMED · synced 25 Oct 2026

Device Name
aerstent
Model / Reference
503-16-060
Primary DI / UDI-DI
14063106100855
Basic UDI-DI
4063106ASTAERLX
EMDN Code
P0401 Tracheobronchial prostheses
Device Class
Class IIb
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006209

Other devices from bess pro gmbh

See all devices from bess pro gmbh →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (12)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: 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

Sources (1)

  • EUDAMED 14063106100855|4063106ASTAERLX 61 fields · synced 25 Oct 2026