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MicroBlate Flex

EUDAMED

Class IIb (EU MDR)

Ref 7-AB1-002

by Creo Medical

Identity

Trade Name
MicroBlate Flex EUDAMED
Device Name
AB1 Electrosurgical Instrument EUDAMED
Model / Reference
7-AB1-002 EUDAMED

Identifiers

Primary DI / UDI-DI
05060359561121 EUDAMED
Basic UDI-DI
506035956MICROBLATEAB13Z 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

MicroBlate Flex 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 (1)

  • EUDAMED 94042222-2271-4ac9-960a-d821c83f6aab 61 fields · synced May 29, 2026