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Pleural Drain Wet Seal System H03004

by CHS USA Incorporated

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 Number00628725095370 UDI-DI Date17 Apr 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  • Withdrawn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
Pleural Drain Wet Seal System
Generic Name
Pleural/peritoneal drainage catheterization kit, non-medicated
Model / Ref / Catalog
H03004
Primary DI / UDI-DI
00628725095370
FDA Product Code
KDQ
GMDN Term
Pleural/peritoneal drainage catheterization kit, non-medicated
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Other devices from CHS USA Incorporated

See all devices from CHS USA Incorporated →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No