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NanoBond

EUDAMED

Class IIa (EU MDR)

Ref P111

by Spident

Identity

Trade Name
NanoBond EUDAMED
Device Name
EsBond EUDAMED
Model / Reference
P111 EUDAMED

Identifiers

Primary DI / UDI-DI
08809911115887 EUDAMED
Basic UDI-DI
B-08809911115887 EUDAMED
880926295EBZF EUDAMED
Direct Marketing DI
08809911115887 EUDAMED
EMDN Code
Q01010104 DENTAL BONDING AGENTS 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

NanoBond by Spident — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

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 bd0a60f0-0947-401f-a0c9-55bc39ef9503 61 fields · synced Jul 9, 2026
  • EUDAMED fb2ff59e-ba8c-489a-b26a-b13bc77616c6 61 fields · synced Jul 9, 2026