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Alfa Wassermann 903394

by Alfa Wassermann, Inc.

Alfa Wassermann 903394 is a Class II device made by Alfa Wassermann, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00857969006044), 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 Number00857969006044 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Alfa Wassermann
Generic name
Potassium (K+) electrode IVD
Model / Ref / Catalog
903394
Primary DI / UDI-DI
00857969006044
FDA product code
CEM
GMDN term
Potassium (K+) electrode IVD
Device class
Class II
Regulation number
862.1600
GUDID distribution status
In Commercial Distribution

Related devices

Category: Potassium (K+) electrode IVD

Similar devices in this category

Other devices filed under Potassium (K+) electrode IVD.

Other devices from Alfa Wassermann, Inc.

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Properties

  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)