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CLEANASCOPE Sterile Tray Liner System

by Steris Italy SRL 2 variants

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 Number00724995356699 UDI-DI Date26 May 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  • Withdrawn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
Cleanascope
Generic Name
Medical equipment/instrument drape, single-use
Model / Ref / Catalog
Sterile Tray Liner System, 4010167
Primary DI / UDI-DI
00724995356699
FDA Product Code
FFY
GMDN Term
Medical equipment/instrument drape, single-use
Device Class
Class I
Regulation Number
876.1500
GUDID distribution status
In Commercial Distribution

Other devices from Steris Italy SRL

See all devices from Steris Italy SRL →

Properties

  • Sterile
  • Single Use
  • Combination Product
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No