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Lasix ONYU 40.00020

by SQ Innovation Inc.

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 Number00381137901317 UDI-DI Date4 Feb 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  • Withdrawn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
Lasix ONYU
Generic Name
Ambulatory non-insulin infusion pump, electronic
Model / Reference
40.00020
Primary DI / UDI-DI
00381137901317
GMDN Term
Ambulatory non-insulin infusion pump, electronic
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from SQ Innovation Inc.

Properties

  • Convenience Kit
  • Combination Product
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No