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EsFlow B1

EUDAMED

Class IIa (EU MDR)

Ref #3304B1

by Spident

Identity

Trade Name
EsFlow B1 EUDAMED
Device Name
EsFlow EUDAMED
Model / Reference
#3304B1 EUDAMED

Identifiers

Primary DI / UDI-DI
08809262954753 EUDAMED
Basic UDI-DI
B-08809262954753 EUDAMED
880926295FI23 EUDAMED
Direct Marketing DI
08809262954753 EUDAMED
EMDN Code
Q01010103 DENTAL RESTORATIVE COMPOSITES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Greece EUDAMED
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

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: Dental composite resin

EsFlow B1 by Spident — Class IIa — MDR, 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/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Spident
EUDAMED SRN
KR-MF-000008691
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (2)

  • EUDAMED 2ba9ab83-4d62-4301-9f5a-0f397a96d37c 61 fields · synced Jul 28, 2026
  • EUDAMED a1105f2c-667f-490d-8bb1-5118db62cac9 61 fields · synced Jul 28, 2026