Skip to content

Zone Valve, Digi-Flo 49550

by Accutron

Zone Valve, Digi-Flo 49550 is a Class I device made by Accutron, listed in FDA GUDID since 22 Sep 2023 (UDI-DI 00813830024753), 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 Number00813830024753 UDI-DI Date22 Sep 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  • Withdrawn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
Zone Valve, Digi-Flo
Generic name
Medical gas pipeline system
Model / Ref / Catalog
49550
Primary DI / UDI-DI
00813830024753
FDA product code
BXH
GMDN term
Medical gas pipeline system
Device class
Class I
Regulation number
868.2610
GUDID distribution status
In Commercial Distribution

Related devices

Category: Medical gas pipeline system

Similar devices

Other devices filed under FDA product code BXH (Gauge, Gas Pressure, Cylinder/Pipeline).

Other devices from Accutron

See all devices from Accutron →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)