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ecoFlow

EUDAMED

Class IIa (EU MDR)

Ref -Model ecoFlow Refill Package A1

by Diadent Group International

Identity

Trade Name
ecoFlow EUDAMED
Device Name
ecoFlow EUDAMED
Model / Reference
ecoFlow Refill Package A1 EUDAMED
- EUDAMED

Identifiers

Primary DI / UDI-DI
08806383591539 EUDAMED
Basic UDI-DI
B-08806383591539 EUDAMED
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Romania EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Dental composite resin

ecoFlow by Diadent Group International — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
KR-MF-000023806
Authorised Representative
Diadent Europe B.V. NL-AR-000012597

Sources (1)

  • EUDAMED d5c92cb0-43a5-453a-9cdf-6b83c7649bc1 61 fields · synced Jul 10, 2026