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Vonflex S Putty

by Vericom Co., Ltd. 16 variants

Part of a family of 20 devices: see the family page

Ref VF356-SPFR

Vonflex S Putty (VF356-SPFR) is a Class I device made by Vericom Co., Ltd., registered in EUDAMED on 23 Sep 2026 (Basic UDI-DI 880925445VFSTM), active as of 7 Nov 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number880925445VFSTM Basic UDI-DI 08809254455107UDI-DIDate23 Sep 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Dental Impression Materials
Model / reference
VF356-SPFR
Primary DI / UDI-DI
08809254455107
Basic UDI-DI
880925445VFSTM
EMDN code
Q01020102 Dental impression vinylsiloxans
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
KR-MF-000012442
Authorised representative
KTR Europe GmbH DE-AR-000005685

Other devices from Vericom Co., Ltd.

See all devices from Vericom Co., Ltd. →

Properties

Other properties (14, all answered No)