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Digitimer DS7AP

by Digitimer, Ltd.

Ref DS7AP

Digitimer DS7AP is a device classified as Class IIa in the EU and Class II in the US made by Digitimer, Ltd., registered in EUDAMED on 8 Sep 2026 (Basic UDI-DI B-05060490360058), cleared under FDA 510(k) K172381 on 6 Mar 2018 and listed in FDA GUDID since 21 Sep 2023 (UDI-DI 05060490360058), active as of 24 Oct 2026.

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

CE MDD 510(k)

Valid until

No date given

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

FDA recalls

None found

in data synced 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K172381

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05060490360058 Basic UDI-DI 05060490360058UDI-DIDate8 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060490360058 UDI-DI Date21 Sep 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK172381 Date6 Mar 2018DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-05060490360058 registered 8 Sep 2026 Active
  • FDA 510(k) K172381 decided 6 Mar 2018 Active
  • FDA GUDID UDI-DI 05060490360058 listed 21 Sep 2023 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K172381
  2. Listed FDA GUDID 05060490360058
  3. Registered EUDAMED B-05060490360058

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Digitimer
Generic name
Diagnostic peripheral nerve electrical stimulation system
Device name
Constant Current High Voltage Stimulator
Model / reference
DS7AP
Primary DI / UDI-DI
05060490360058
Basic UDI-DI
B-05060490360058
510(k) Number
FDA product code
GWF
EMDN code
Z12101106 Neurological stimulators
GMDN term
Diagnostic peripheral nerve electrical stimulation system
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
882.1870
EU registration type
Legacy device (under a directive)
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Diagnostic peripheral nerve electrical stimulation system

Similar devices in this category

Other devices filed under NEUROLOGICAL STIMULATORS.

Other devices from Digitimer, Ltd.

See all devices from Digitimer, Ltd. →

Properties

  • Serial number
  • Manufacturing date
Other properties (21, all answered No)