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Pruitt® Occlusion Catheter

EUDAMED

Class IIa (EU MDR)

Ref 2103-56MRef 2103-36MRef 2103-46M

by LeMaitre Vascular, Inc.

Identity

Trade Name
Pruitt® Occlusion Catheter EUDAMED
Device Name
Pruitt® Occlusion Catheter EUDAMED
Model / Reference
2103-56M EUDAMED
2103-36M EUDAMED
2103-46M EUDAMED

Identifiers

Primary DI / UDI-DI
00840663111336 EUDAMED
00840663111312 EUDAMED
00840663111329 EUDAMED
Basic UDI-DI
08406631POCUZ EUDAMED
EMDN Code
C0104020103 VASCULAR OCCLUSION CATHETERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Pruitt® Occlusion Catheter by LeMaitre Vascular, Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (3)

  • EUDAMED 46c46757-f85d-490e-9536-d6e6f0eb1acd 61 fields · synced Jul 29, 2026
  • EUDAMED 00b90730-1cee-4505-a4f0-cb782c358769 61 fields · synced May 17, 2026
  • EUDAMED 3e41bb77-3093-4459-aaee-92728461b33e 61 fields · synced May 18, 2026