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Pg-1018

by Boston Scientific Neuromodulation

Ref PG-1018

Pg-1018 is a device classified as Class I in the EU and Class II in the US made by Boston Scientific Neuromodulation, registered in EUDAMED on 1 May 2026 (Basic UDI-DI 01915060000000000000179NC) and listed in FDA GUDID since 17 Dec 2018 (UDI-DI 00813250017083), active as of 22 Oct 2026.

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

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number01915060000000000000179NC Basic UDI-DI 00813250017083UDI-DIDate1 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00813250017083 UDI-DI Date17 Dec 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 01915060000000000000179NC registered 1 May 2026 Active
  • FDA GUDID UDI-DI 00813250017083 listed 17 Dec 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00813250017083
  2. Registered EUDAMED 01915060000000000000179NC

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  • Withdrawn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

Trade name
Palisade™
Generic name
Radio-frequency ablation system
Device name
Palisade Guide Block
Model / reference
PG-1018
Primary DI / UDI-DI
00813250017083
Basic UDI-DI
01915060000000000000179NC
FDA product code
GXI
EMDN code
K020380 Devices for surgery with radiofrequency generator, single-use - accessories
GMDN term
Radio-frequency ablation system
Device class
Class I EUDAMED
Class II GUDID
Regulation number
882.4725
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Radio-frequency ablation system

Similar devices in this category

Other devices filed under DEVICES FOR SURGERY WITH RADIOFREQUENCY GENERATOR, SINGLE-USE - ACCESSORIES.

Other devices from Boston Scientific Neuromodulation

See all devices from Boston Scientific Neuromodulation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)