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Speedboat Inject

EUDAMED

Class IIb (EU MDR)

Ref 7-RS2-001Ref 7-RS2-003

by Creo Medical

Identity

Trade Name
Speedboat Inject EUDAMED
Device Name
Speedboat Electrosurgical Instrument EUDAMED
Model / Reference
7-RS2-001 EUDAMED
7-RS2-003 EUDAMED

Identifiers

Primary DI / UDI-DI
05060359560766 EUDAMED
05060359560735 EUDAMED
Basic UDI-DI
506035956SPEEDBOATINRS2G3 EUDAMED
EMDN Code
K0299 ELECTROSURGERY DEVICES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain 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: Percutaneous radio-frequency ablation system generator

Speedboat Inject by Creo Medical — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation system generator.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Creo Medical
EUDAMED SRN
GB-MF-000019076
Authorised Representative
Creo Medical, S.L.U. ES-AR-000001355

Sources (2)

  • EUDAMED 99e37a50-090e-4615-83b6-1a0c38e18ec3 61 fields · synced Jul 26, 2026
  • EUDAMED 1c262bfe-c6df-41da-ba1e-ad6baed2096b 61 fields · synced May 18, 2026