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Jazz

EUDAMEDFDA 510(k)

Class IIa (EU MDR)

Ref JAZZ

by AI Medical AG

Identity

Trade Name
JAZZ EUDAMED
Device Name
Jazz EUDAMED
Model / Reference
JAZZ EUDAMED

Identifiers

Primary DI / UDI-DI
07649990295015 EUDAMED
Basic UDI-DI
7649990295JAZZNJ EUDAMED
Direct Marketing DI
07649990295015 EUDAMED
EMDN Code
Z11030592 RADIOLOGY INSTRUMENTS - MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Netherlands 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

Jazz by AI Medical AG — Class IIa — 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
AI Medical AG
EUDAMED SRN
CH-MF-000026860
Authorised Representative
MED-RAS GmbH Regulatory Affairs Service DE-AR-000006211

Sources (2)

  • EUDAMED 8b3e9e2d-19ab-43f1-9bc6-96ca97813f29 61 fields · synced Jun 18, 2026
  • FDA 510(k) K223659 1 fields · synced May 18, 2026