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DRY320

by Wassenburg Medical, Inc. 2 variants

DRY320 is a Class I device made by Wassenburg Medical, Inc., listed in FDA GUDID since 23 Apr 2024 (UDI-DI 00860010835234), 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 Number00860010835234 UDI-DI Date23 Apr 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  • Withdrawn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
Endoscope drying/storage cabinet
Model / reference
DRY320
Primary DI / UDI-DI
00860010835234
FDA product code
JRJ
GMDN term
Endoscope drying/storage cabinet
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscope drying/storage cabinet

Other devices from Wassenburg Medical, Inc.

See all devices from Wassenburg Medical, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)