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Tigertriever 25 Revascularization Device

EUDAMEDFDA 510(k)

Class III (EU MDR)

Ref TRPP3125

by Rapid Medical Ltd

Identity

Trade Name
Tigertriever 25 Revascularization Device EUDAMED
Device Name
Tigertriever Revascularization Device EUDAMED
Model / Reference
TRPP3125 EUDAMED

Identifiers

Primary DI / UDI-DI
07290015107310 EUDAMED
Basic UDI-DI
7290015107TRPP13C EUDAMED
Direct Marketing DI
07290015107310 EUDAMED
EMDN Code
C019010 INTRAVASCULAR RECANALISATION SYSTEMS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

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

Category: Vascular graft tunneller

Tigertriever 25 Revascularization Device by Rapid Medical Ltd — Class III — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Similar devices

Also classified as Vascular graft tunneller.

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Rapid Medical Ltd
EUDAMED SRN
IL-MF-000012181
Authorised Representative
MedNet EC-REP III GmbH DE-AR-000011191

Sources (2)

  • EUDAMED 5d16b35f-0f92-48d0-910d-3ade58cc8004 61 fields · synced Jul 9, 2026
  • FDA 510(k) K253062 1 fields · synced May 18, 2026