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MapRT 1.2.x Clearance Mapping

by Vision RT Ltd.

Ref MapRT

MapRT 1.2.x Clearance Mapping is a medical device (EU MDR Class IIb; FDA Class II; FDA product code IYE, Accelerator, Linear, Medical; EMDN category various radiotherapy and radiosurgery instruments) made by Vision RT Ltd., registered in EUDAMED on 9 Mar 2026 (Basic UDI-DI 5056190500764VP), cleared under FDA 510(k) K243301 on 19 May 2025 and listed in FDA GUDID since 23 Dec 2025 (UDI-DI 05056190501044), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K243301

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number5056190500764VP Basic UDI-DI 05056190501044UDI-DIDate9 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05056190501044 UDI-DI Date23 Dec 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k) GUDID from GUDID NumberK243301 Date19 May 2025IssuedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 5056190500764VP registered 9 Mar 2026 Active
  • FDA 510(k) K243301 decided 19 May 2025 Active
  • FDA GUDID UDI-DI 05056190501044 listed 23 Dec 2025 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K243301
  2. Listed FDA GUDID 05056190501044
  3. Registered EUDAMED 5056190500764VP

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
MapRT 1.2.x Clearance Mapping EUDAMED
MapRT GUDID
Generic name
Radiological video camera patient positioning/tracking system
Model / reference
MapRT EUDAMED
MapRT Mapping application (v1.2) GUDID
Primary DI / UDI-DI
05056190501044
Basic UDI-DI
5056190500764VP
Direct marketing DI
05056190501044
510(k) Number
FDA product code
IYE
EMDN code
Z11019099 Various radiotherapy and radiosurgery instruments - other
GMDN term
Radiological video camera patient positioning/tracking system
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 · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MapRT
GUDID
MapRT Mapping application (v1.2)
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.

Manufacturer details

EUDAMED SRN
GB-MF-000010499
Authorised representative
Oticon A/S DK-AR-000006135

Similar devices in this category

Other devices filed under VARIOUS RADIOTHERAPY AND RADIOSURGERY INSTRUMENTS - OTHER.

Other devices from Vision RT Ltd.

See all devices from Vision RT Ltd. →

Properties

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