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Tornado G47545

by Cook Incorporated

Listed FDA GUDID listing, no authorization on record

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00827002475458 UDI-DI Date4 Sep 2018ListedStatusListed GUDID: 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  • Withdrawn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
Tornado
Generic Name
Non-neurovascular embolization coil
Model / Ref / Catalog
G47545, MWCE-38-8/5-TORNADO-01
Primary DI / UDI-DI
00827002475458
FDA Product Code
KRD
GMDN Term
Non-neurovascular embolization coil
Device Class
Class II
Regulation Number
870.3300
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Non-neurovascular embolization coil

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No