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StingRay DP60-000

by IBA Dosimetry GmbH

Ref DP60-000

StingRay DP60-000 is a device classified as Class IIb in the EU and Class II in the US made by IBA Dosimetry GmbH, registered in EUDAMED on 17 Jul 2026 (Basic UDI-DI ++EIBASTINGRAYRG) and listed in FDA GUDID since 9 Sep 2016 (UDI-DI EIBADP600000), 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 Number++EIBASTINGRAYRG Basic UDI-DI EIBADP600000UDI-DIDate17 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberEIBADP600000 UDI-DI Date9 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI ++EIBASTINGRAYRG registered 17 Jul 2026 Active
  • FDA GUDID UDI-DI EIBADP600000 listed 9 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID EIBADP600000
  2. Registered EUDAMED ++EIBASTINGRAYRG

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  • Withdrawn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
StingRay
Generic name
Radiation electrometer
Model / reference
DP60-000
Primary DI / UDI-DI
EIBADP600000
Basic UDI-DI
++EIBASTINGRAYRG
Direct marketing DI
EIBADP600000
FDA product code
IYE
EMDN code
Z119002 Dosimeters
GMDN term
Radiation electrometer
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
892.5050
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb 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: Radiation electrometer

Similar devices in this category

Other devices filed under VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS.

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Properties

  • Reusable
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)