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Ivotion Base Print 746306

by Ivoclar Vivadent Aktiengesellschaft

Ref 746306

Ivotion Base Print 746306 is a device classified as Class IIa in the EU and Class II in the US made by Ivoclar Vivadent Aktiengesellschaft, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 76152082APROS006W5) and listed in FDA GUDID since 12 Feb 2025 (UDI-DI 07615208454901), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number76152082APROS006W5 Basic UDI-DI 07615208454901UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07615208454901 UDI-DI Date12 Feb 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 76152082APROS006W5 registered 21 May 2026 Active
  • FDA GUDID UDI-DI 07615208454901 listed 12 Feb 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07615208454901
  2. Registered EUDAMED 76152082APROS006W5

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Ivotion Base Print Pink 1000ml EUDAMED
Ivotion Base Print GUDID
Generic name
Dental appliance fabrication material, resin
Model / Ref / Catalog
746306
Primary DI / UDI-DI
07615208454901
Basic UDI-DI
76152082APROS006W5
FDA product code
EBI
EMDN code
Q010699 Materials for the preparation of custom-made dental devices - other
GMDN term
Dental appliance fabrication material, resin
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3760
EU registration type
Standard device
EU market of registration
Liechtenstein
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Dental appliance fabrication material, resin

Similar devices in this category

Other devices filed under MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER.

Other devices from Ivoclar Vivadent Aktiengesellschaft

See all devices from Ivoclar Vivadent Aktiengesellschaft →

Properties

  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (21, all answered No)