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Vmat Pro Aesthetic

EUDAMEDFDA 510(k)

Class IIb (EU MDR)

Ref VMAT PRO AESTHETIC

by Termosalud, S.L.

Identity

Trade Name
VMAT PRO AESTHETIC EUDAMED
Device Name
VMAT PRO AESTHETIC EUDAMED
Model / Reference
VMAT PRO AESTHETIC EUDAMED

Identifiers

Primary DI / UDI-DI
08436601290342 EUDAMED
Basic UDI-DI
843660129SWTSMU EUDAMED
EMDN Code
Z12139001 SHOCK WAVE THERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

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

Vmat Pro Aesthetic by Termosalud, S.L. — Class IIb — FDA_510K, MDR — listed in EUDAMED, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Termosalud, S.L.
EUDAMED SRN
ES-MF-000019177

Sources (2)

  • EUDAMED 7f06e524-61e5-4741-ba35-0bb632f9e82c 61 fields · synced Jul 20, 2026
  • FDA 510(k) K243488 1 fields · synced May 18, 2026