← Back to catalogue

Hexa-Temp A1

EUDAMED

Class IIa (EU MDR)

Ref #1204A1

by Spident

Identity

Trade Name
Hexa-Temp A1 EUDAMED
Device Name
Hexa-Temp EUDAMED
Model / Reference
#1204A1 EUDAMED

Identifiers

Primary DI / UDI-DI
08809262953701 EUDAMED
Basic UDI-DI
880926295HX37 EUDAMED
Direct Marketing DI
08809262953701 EUDAMED
EMDN Code
Q0102050101 TEMPORARY TEETH RESINS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

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: Dental appliance fabrication material, resin

Hexa-Temp A1 by Spident — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED a56639fc-10f3-410d-9329-588a18319e9e 61 fields · synced Jun 18, 2026