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Pruitt® Occlusion Catheter

by LeMaitre Vascular, Inc. United States EUDAMED

Ref 2103-36M EMDN C0104020103

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08406631POCUZ Basic UDI-DIDate24 Sep 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Model / Reference
2103-36M
Primary DI / UDI-DI
00840663111312
Basic UDI-DI
08406631POCUZ
EMDN Code
C0104020103 Vascular occlusion catheters
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000016778
Authorised representative
LeMaitre Vascular GmbH DE-AR-000013539

From the manufacturer

Manufacturer's product page: Pruitt® Occlusion Catheters

Other devices from LeMaitre Vascular, Inc.

See all devices from LeMaitre Vascular, Inc. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Contains Latex
Other properties (11)
  • Implantable: No
  • Reusable: 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 00b90730-1cee-4505-a4f0-cb782c358769 61 fields · synced 25 Oct 2026