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KeyPrint 4220406

by Keystone Industries

Ref 4220406

KeyPrint 4220406 is a Class I device made by Keystone Industries, registered in EUDAMED on 4 May 2026 (Basic UDI-DI ++H6683DTRYIN001QT) and listed in FDA GUDID since 30 Nov 2022 (UDI-DI ++H66842204061), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number++H6683DTRYIN001QT Basic UDI-DI ++H66842204061UDI-DIDate4 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number++H66842204061 UDI-DI Date30 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++H6683DTRYIN001QT registered 4 May 2026 Active
  • FDA GUDID UDI-DI ++H66842204061 listed 30 Nov 2022 Listed

Certificates

0 certificates · EUDAMED

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

Timeline

2 dated events

  1. Listed FDA GUDID ++H66842204061
  2. Registered EUDAMED ++H6683DTRYIN001QT

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  • Withdrawn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
KeyDentureTry-In EUDAMED
KeyPrint GUDID
Generic name
Dental appliance fabrication material, resin
Device name
3D resin for printed Try-In Dentures
Model / Ref / Catalog
4220406
Primary DI / UDI-DI
++H66842204061 EUDAMED
H66842204061 GUDID
Basic UDI-DI
++H6683DTRYIN001QT
FDA product code
EBH
EMDN code
Q0102050199 Dentistry resins - other
GMDN term
Dental appliance fabrication material, resin
Device class
Class I
Regulation number
872.3670
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Weight — 1 Kilogram
Total Volume — 35.3 Fluid Ounce

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
++H66842204061
GUDID
H66842204061

The registries describe this device under different primary UDI-DIs (EUDAMED lists ++H66842204061; FDA GUDID lists H66842204061), so their flags are not compared.

Related devices

Category: Dental appliance fabrication material, resin

Similar devices in this category

Other devices filed under DENTISTRY RESINS - OTHER.

Other devices from Keystone Industries

See all devices from Keystone Industries →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)