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ScanNav Anatomy: Peripheral Nerve Block

by Intelligent Ultrasound Limited

Ref v4.0

Active Active in United States. Withdrawn in European Union.

CE MDR, withdrawn 510(k) De Novo

Valid until

No expiry

FDA authorization is 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) K232787↗

+1 more

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k) 510(k) NumberK232787 Date6 Oct 2023IssuedStatusActive
European UnionCE/MDR EUDAMED Number506087881IU00187 Basic UDI-DI 05060878810090UDI-DIDate26 Jan 2023RegisteredStatusWithdrawn No longer placed on the EU market
United StatesFDA De Novo De Novo NumberDEN220024 Date18 Oct 2022IssuedStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

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  • Withdrawn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  • European Union CE/MDR Withdrawn

Specification

EUDAMED · 510(k)

Model / Reference
v4.0
Primary DI / UDI-DI
05060878810090
Basic UDI-DI
506087881IU00187
EMDN Code
Z11069092 Various digital bioimaging management instruments - medical device software
Device Class
Class IIa
Special Device Type
Software
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
GB-MF-000002764
Authorised representative
Advena Limited MT-AR-000000234

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No