Skip to content

Viewer, 5.3

by Brainlab SE

Ref 04056481143800

Viewer, 5.3 (04056481143800) is a device classified as Class IIb in the EU and Class II in the US made by Brainlab SE, registered in EUDAMED on 30 Jun 2025 (Basic UDI-DI 4056481ViewerPW), cleared under FDA 510(k) K191014 on 23 Jan 2020 and listed in FDA GUDID since 30 Mar 2022 (UDI-DI 04056481143800), 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) K191014

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 Number4056481ViewerPW Basic UDI-DI 04056481143800UDI-DIDate30 Jun 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04056481143800 UDI-DI Date30 Mar 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK191014 Date23 Jan 2020DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 4056481ViewerPW registered 30 Jun 2025 Active
  • FDA 510(k) K191014 decided 23 Jan 2020 Active
  • FDA GUDID UDI-DI 04056481143800 listed 30 Mar 2022 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K191014
  2. Listed FDA GUDID 04056481143800
  3. Registered EUDAMED 4056481ViewerPW

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  • Withdrawn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
Viewer, 5.3 EUDAMED
Viewer GUDID
Generic name
Medical image management system
Model / reference
04056481143800 EUDAMED
5.3 GUDID
Primary DI / UDI-DI
04056481143800
Basic UDI-DI
4056481ViewerPW
Direct marketing DI
04056481143800
510(k) Number
FDA product code
LLZ
EMDN code
Z11069092 Various digital bioimaging management instruments - medical device software
GMDN term
Medical image management system
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
892.2050
Special device type
Software
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
04056481143800
GUDID
5.3
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
DE-MF-000006183

Similar devices in this category

Other devices filed under VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - MEDICAL DEVICE SOFTWARE.

Other devices from Brainlab SE

See all devices from Brainlab SE →

Properties

  • Prescription use
  • Lot / batch number
Other properties (23, all answered No)