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cytoQ® Non-Gyn Filters

by SABEU GmbH & Co. KG

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 Number04260649292099 UDI-DI Date10 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  • Withdrawn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
cytoQ®
Generic Name
Fluid specimen concentration filter IVD
Model / Ref / Catalog
cytoQ® Non-Gyn Filters, 968112
Primary DI / UDI-DI
04260649292099
FDA Product Code
KET
GMDN Term
Fluid specimen concentration filter IVD
Device Class
Class I
Regulation Number
864.3010
GUDID distribution status
In Commercial Distribution

Other devices from SABEU GmbH & Co. KG

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No