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Polofil Supra N

by VOCO GmbH 4 variants

Ref 1410, 1374, 1362, 1361, 1413, 1415, 1375, 1417, 1368, 1412, 1363, 1366

Polofil Supra N (1410) is a Class IIa device made by VOCO GmbH, registered in EUDAMED on 30 Mar 2026 (Basic UDI-DI ++E22100600100000008E), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++E22100600100000008E Basic UDI-DI Date30 Mar 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade name
Polofil Supra N
Polofil Supra
Model / reference
1410, 1374, 1362, 1361, 1413, 1415, 1375, 1417, 1368, 1412, 1363, 1366
Primary DI / UDI-DI
E22114101, E22113741, E22113621, E22113611, E22114131, E22114151, E22113751, E22114171, E22113681, E22114121, E22113631, E22113661
Basic UDI-DI
++E22100600100000008E, ++E22100600000000007T
EMDN code
Q01010103 Dental restorative composites
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000008601

Related devices

Category: Dental composite resin

Similar devices in this category

Other devices filed under DENTAL RESTORATIVE COMPOSITES.

Other devices from VOCO GmbH

See all devices from VOCO GmbH →

Properties

  • Implantable
Other properties (13, all answered No)