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HTx Procedure Pack

by Suzhou AcuVu medical technology Co., Ltd.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06974880991427 UDI-DI Date28 Jun 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  • Withdrawn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/irrigation tubing, single-use
Model / Reference
inflow tubing+ drainage fluid tube + under buttocks drape
Primary DI / UDI-DI
06974880991427
FDA Product Code
NWW
GMDN Term
Suction/irrigation tubing, single-use
Device Class
Class I
Regulation Number
884.1690
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suction/irrigation tubing, single-use

Other devices from Suzhou AcuVu medical technology Co., Ltd.

See all devices from Suzhou AcuVu medical technology Co., Ltd. →

Properties

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

Other properties (7)

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