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myQA®Daily E3063100

by IBA Dosimetry GmbH

Ref DQ01-000

myQA®Daily E3063100 is a device classified as Class IIb in the EU and Class I in the US made by IBA Dosimetry GmbH, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI ++EIBAMYQADAILY4L) and listed in FDA GUDID since 25 Apr 2019 (UDI-DI EIBAE30631000), 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 Number++EIBAMYQADAILY4L Basic UDI-DI EIBAE30631000UDI-DIDate16 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEIBAE30631000 UDI-DI Date25 Apr 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++EIBAMYQADAILY4L registered 16 Oct 2026 Active
  • FDA GUDID UDI-DI EIBAE30631000 listed 25 Apr 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EIBAE30631000
  2. Registered EUDAMED ++EIBAMYQADAILY4L

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  • Withdrawn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
myQA®Daily
Generic name
Accelerator system quality assurance device
Device name
myQA Daily
Model / reference
DQ01-000 EUDAMED
E3063100 GUDID
Primary DI / UDI-DI
EIBAE30631000
Basic UDI-DI
++EIBAMYQADAILY4L
Direct marketing DI
EIBAE30631000
FDA product code
LHO
EMDN code
Z119002 Dosimeters
GMDN term
Accelerator system quality assurance device
Device class
Class IIb EUDAMED
Class I GUDID
Regulation number
892.1940
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
DQ01-000
GUDID
E3063100
Device classEUDAMED
Class IIb
GUDID
Class I

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

Related devices

Category: Accelerator system quality assurance device

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Properties

  • Measuring function
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)