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DCI Standard Vacuum Valve

by DCI International, LLC

DCI Standard Vacuum Valve is a Class I device made by DCI International, LLC, listed in FDA GUDID since 7 Jul 2023 (UDI-DI 00810021431178), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810021431178 UDI-DI Date7 Jul 2023ListedStatusListed 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  • Withdrawn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

Trade name
Dci
Generic name
Dental suction system cannula, reusable
Model / reference
Standard Vacuum Valve
Primary DI / UDI-DI
00810021431178
FDA product code
EHZ
GMDN term
Dental suction system cannula, reusable
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental suction system cannula, reusable

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See all devices from DCI International, LLC →

Properties

  • Sterilise before use
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)