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Suction Liner

by Shijiazhuang Yuanding Medical Device Co., LTD 21 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 7 Oct 2026. What this means

Regulatory status

as of registry sync 7 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971092631592 UDI-DI Date28 Feb 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Suction system canister liner
Model / Ref / Catalog
YDB Suction liner without shutoff filter with solidifying agent 2000ml, YDB0120
Primary DI / UDI-DI
06971092631592
FDA Product Code
KDQ
GMDN Term
Suction system canister liner
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 2000 Milliliter

Other devices from Shijiazhuang Yuanding Medical Device Co., LTD

See all devices from Shijiazhuang Yuanding Medical Device Co., LTD →

Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No