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Tycheseal™

by Beijing Percutek Therapeutics Inc. China EUDAMED

Ref PTBS2222210Model PTBS

EMDN P070401010102

Regulatory status

as of 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06957485020419 Basic UDI-DIDate23 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Tycheseal™ Thoracic stent graft system
Model / Reference
PTBS, PTBS2222210
Primary DI / UDI-DI
06957485020419
Basic UDI-DI
B-06957485020419
EMDN Code
P070401010102 Dacron vascular endoprostheses, straight - thoracic
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000013927
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Beijing Percutek Therapeutics Inc.

See all devices from Beijing Percutek Therapeutics Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • 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

Sources (1)

  • EUDAMED 681607ea-e1db-439d-9441-7636ee6baa7b 61 fields · synced 22 Oct 2026