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EsTemp C&B A1

by Spident

Part of a family of 18 devices: see the family page

Ref #E1204A1

EsTemp C&B A1 (#E1204A1) is a Class IIa device made by Spident, registered in EUDAMED on 2 Apr 2026 (Basic UDI-DI 880926295HX37), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880926295HX37 Basic UDI-DI 08809911114507UDI-DIDate2 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Hexa-Temp
Model / reference
#E1204A1
Primary DI / UDI-DI
08809911114507
Basic UDI-DI
880926295HX37
Direct marketing DI
08809911114507
EMDN code
Q0102050101 Temporary teeth resins
Device class
Class IIa
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
KR-MF-000008691
Authorised representative
AR Experts B.V. NL-AR-000023989

Similar devices in this category

Other devices filed under TEMPORARY TEETH RESINS.

Other devices from Spident

See all devices from Spident →

Properties

Other properties (14, all answered No)