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Suction Liner

by Shijiazhuang Yuanding Medical Device Co., LTD 21 variants

Suction Liner (YDC0020) is a suction system canister liner (FDA Class II; FDA product code KDQ, Bottle, Collection, Vacuum) made by Shijiazhuang Yuanding Medical Device Co., LTD, listed in FDA GUDID since 28 Feb 2024 (UDI-DI 06971092631646), registry data as of 21 Oct 2026.

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

Source GUDID, synced 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06971092631646 UDI-DI Date28 Feb 2024ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
YDC suction liner without shutoff filter 2000ml, YDC0020
Primary DI / UDI-DI
06971092631646
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

Similar devices in this category

Other devices filed under Suction system canister liner.

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 (10, all answered No)