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Idb 3 Sri-0202219

by Sprintray, Inc.

Ref SRI-0202219

Idb 3 Sri-0202219 is a Class I device made by Sprintray, Inc., registered in EUDAMED on 5 May 2026 (Basic UDI-DI 0850070544SRI-0202219DB) and listed in FDA GUDID since 17 Mar 2026 (UDI-DI 00850070544832), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0850070544SRI-0202219DB Basic UDI-DI 00850070544832UDI-DIDate5 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850070544832 UDI-DI Date17 Mar 2026ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0850070544SRI-0202219DB registered 5 May 2026 Active
  • FDA GUDID UDI-DI 00850070544832 listed 17 Mar 2026 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00850070544832
  2. Registered EUDAMED 0850070544SRI-0202219DB

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  • Withdrawn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
Idb 3
Generic name
Dental appliance fabrication material, resin
Model / reference
SRI-0202219
Primary DI / UDI-DI
00850070544832
Basic UDI-DI
0850070544SRI-0202219DB
FDA product code
QJJ
EMDN code
Q0102050199 Dentistry resins - other
GMDN term
Dental appliance fabrication material, resin
Device class
Class I
Regulation number
872.5410
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Other devices from Sprintray, Inc.

See all devices from Sprintray, Inc. →

Properties

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