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SQUID Liquid Embolic Agent SQUID12KIT

by Balt USA LLC

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 Number00840303707295 UDI-DI Date23 Jun 2026ListedStatusListed 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  • Withdrawn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
SQUID Liquid Embolic Agent
Generic Name
Neurovascular embolization plug
Model / Ref / Catalog
SQUID12KIT
Primary DI / UDI-DI
00840303707295
FDA Product Code
SGU
GMDN Term
Neurovascular embolization plug
Device Class
Class III
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Other devices from Balt USA LLC

See all devices from Balt USA LLC →

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