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Na 7885

by Advanced Neuromodulation Systems

Ref 7885

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

4 Jul 2031

CE MDR certificate

FDA recalls

None found

in data synced 24 Oct 2026

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number5415067DRG0001E4 Basic UDI-DI 05415067029072UDI-DIDate13 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05415067029072 UDI-DI Date16 Nov 2017ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 725783 Active Reissued

    Technical documentation EU MDR

    Certifier
    BSI Group The Netherlands B.V. 2797
    Issued
    30 Jun 2026
    Expires
    4 Jul 2031
    Valid from
    4 Jul 2026

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

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  • Withdrawn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

Generic Name
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Device Name
Dorsal Root Ganglion Stimulation
Model / Ref / Catalog
7885
Primary DI / UDI-DI
05415067029072
Basic UDI-DI
5415067DRG0001E4
PMA Number
FDA Product Code
PMP
EMDN Code
Z12101185 Peripheral or central neuro stimulation and assessment instruments - consumables
GMDN Term
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Device Class
Class III
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
ImplantableEUDAMED
Yes
GUDID
No

Related devices

Category: Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator

Cleared under the same submission (P150004)

Show all (12)

Other devices from Advanced Neuromodulation Systems

See all devices from Advanced Neuromodulation Systems →

Properties

  • Single Use
  • Implantable YesEUDAMEDNoGUDID
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (19)

  • Sterile: 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No