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System 83 Plus 2

by Wassenburg Medical, Inc. 2 variants

System 83 Plus 2 is a Class II device made by Wassenburg Medical, Inc., listed in FDA GUDID since 15 Aug 2023 (UDI-DI G434SYSTEM83PLUS2), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG434SYSTEM83PLUS2 UDI-DI Date15 Aug 2023ListedStatusListed 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  • Withdrawn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
System 83 Plus
Generic name
Instrument non-thermal chemical disinfector
Model / reference
SYSTEM 83 PLUS 2
Primary DI / UDI-DI
G434SYSTEM83PLUS2
FDA product code
FEB
GMDN term
Instrument non-thermal chemical disinfector
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FEB (Accessories, Cleaning, For Endoscope).

Other devices from Wassenburg Medical, Inc.

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Properties

  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)