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SNC Phantom (WL-QA) 1253300

by Sun Nuclear Corporation

Ref 1253 WL-QAModel 1253

SNC Phantom (WL-QA) 1253300 is a Class I device made by Sun Nuclear Corporation, registered in EUDAMED on 16 Jan 2026 (Basic UDI-DI 506060888PHWLPHGT) and listed in FDA GUDID since 22 Jul 2020 (UDI-DI 05060608880966), 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 Number506060888PHWLPHGT Basic UDI-DI 05060608880966UDI-DIDate16 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060608880966 UDI-DI Date22 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 506060888PHWLPHGT registered 16 Jan 2026 Active
  • FDA GUDID UDI-DI 05060608880966 listed 22 Jul 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060608880966
  2. Registered EUDAMED 506060888PHWLPHGT

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  • Withdrawn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
SNC Phantom WL-QA EUDAMED
SNC Phantom (WL-QA) GUDID
Generic name
Accelerator system quality assurance device
Model / Ref / Catalog
1253 EUDAMED
1253 WL-QA EUDAMED
1253300 GUDID
Primary DI / UDI-DI
05060608880966
Basic UDI-DI
506060888PHWLPHGT
FDA product code
IXG
EMDN code
Z11030599 Radiology instruments - other
GMDN term
Accelerator system quality assurance device
Device class
Class I
Regulation number
892.1950
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
Model / referenceEUDAMED
1253
1253 WL-QA
GUDID
1253300

Related devices

Category: Accelerator system quality assurance device

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Properties

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