Skip to content

Myerson db plus T30C4U0R40

by The Myerson Company Limited

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

CE MDR

Valid until

16 Oct 2030

CE MDR certificate

FDA recalls

None found

in data synced 28 Oct 2026

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 28 Oct 2026. What this means

Regulatory status

as of registry sync 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number28620225594 Date17 Oct 2025IssuedStatusActive expires 16 Oct 2030
United StatesGUDID listing GUDID Number00842326135451 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 28 Oct 2026.

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  • Withdrawn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
Myerson db plus
Generic Name
Resin artificial teeth
Model / Reference
T30C4U0R40, T30A2U0R41, T30A1U0T76, T30A2L0L13, T30A1U0R41, T30A1U0T40, T30A1U0O45, T30A1L0L16, T30A2L00L8, T30A1L0L15, T30A2U0S79, T30A1L00L8, T30A1U0R69, T30A2U0O40, T30A1L00L6, T30A2U0R88, T30D3U0O65, T30A2L0L11, T30A2U0R58, T30A2U0T43, T30A1U0T90, T30A2U0R61, T30A1U0S83, T30A2U0O55, T30A2U0T90, T30A1U0O65, T30A1U0O89, T30A1U0S71, T30A2U0S98, T30A2U0O99, T30A2U0S56, T30A2L00L7, T30A1U0S65, T30A2U0R78, T30A2U0T40, T30A1U0O99, T30A1U0R88, T30A1U0T54, T30A2U0T63, T30A2U0R40, T30A1L00L3, T30A1L0L11, T30A1L0L13, T30A2U0T53, T30A1U0O80, T30A2L00L5, T30A2U0T81, T30A2U0O45, T30A2L00L6, T30A1U0S79, T30A1U0O55
Primary DI / UDI-DI
00842326135451, 00842326130623, 00842326130142, 00842326130852, 00842326130180, 00842326130098, 00842326130012, 00842326130432, 00842326130821, 00842326130425, 00842326130746, 00842326130388, 00842326130210, 00842326130449, 00842326130364, 00842326130678, 00842326136205, 00842326130845, 00842326130630, 00842326130548, 00842326130166, 00842326130647, 00842326130319, 00842326130470, 00842326130609, 00842326130043, 00842326130074, 00842326130296, 00842326130760, 00842326130524, 00842326130708, 00842326130814, 00842326130272, 00842326130661, 00842326130531, 00842326130081, 00842326130234, 00842326130128, 00842326130579, 00842326130616, 00842326130340, 00842326130401, 00842326130418, 00842326130555, 00842326130067, 00842326130791, 00842326130593, 00842326130456, 00842326130807, 00842326130302, 00842326130036
510(k) Number
FDA Product Code
ELM
GMDN Term
Resin artificial teeth
Device Class
Class II
Regulation Number
872.3590
GUDID distribution status
In Commercial Distribution

Related devices

Category: Resin artificial teeth

Cleared under the same submission (K924526)

Show all (12)

Other devices from The Myerson Company Limited

See all devices from The Myerson Company Limited →

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No