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PulseRider Aneurysm Neck Reconstruction Device Connection Cable PRDSACD

by Medos International Sàrl

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00859030005260 UDI-DI Date17 Sep 2019ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
PulseRider Aneurysm Neck Reconstruction Device Connection Cable
Generic Name
Bare-metal intracranial vascular stent
Model / Ref / Catalog
PRDSACD
Primary DI / UDI-DI
00859030005260
FDA Product Code
NJE
GMDN Term
Bare-metal intracranial vascular stent
Device Class
Unclassified
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No