← Back to catalogue

VasQ Model Selection Tool

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref FG024

by Laminate Medical Technologies Ltd.

Identity

Trade Name
VasQ Model Selection Tool EUDAMED
Device Name
Disposable Model Selection Tool (DMST) EUDAMED
Model / Reference
FG024 EUDAMED

Identifiers

Primary DI / UDI-DI
07290016063240 EUDAMED
Basic UDI-DI
7290016063DMSTEU62 EUDAMED
EMDN Code
C0699 CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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: Surgical bulldog clamp, single-use

VasQ Model Selection Tool by Laminate Medical Technologies Ltd — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Similar devices

Also classified as Surgical bulldog clamp, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

United States Active

FDA_510K

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IL-MF-000009312
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (2)

  • EUDAMED 7ab4cdd5-d72f-4d2b-9c9a-4a806a6ae3a3 61 fields · synced Jul 9, 2026
  • FDA 510(k) K240119 1 fields · synced May 18, 2026