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pH Electrode 3111717180

by Roche Diagnostics GmbH

pH Electrode 3111717180 is a Class II device made by Roche Diagnostics GmbH, listed in FDA GUDID since 20 Sep 2016 (UDI-DI 04015630014248), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04015630014248 UDI-DI Date20 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  • Withdrawn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
pH Electrode
Generic name
Laboratory pH electrode
Model / Ref / Catalog
3111717180
Primary DI / UDI-DI
04015630014248
FDA product code
CHL
GMDN term
Laboratory pH electrode
Device class
Class II
Regulation number
862.1120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Laboratory pH electrode

Similar devices

Other devices filed under FDA product code CHL (ELECTRODE MEASUREMENT, BLOOD-GASES (PCO2, PO2) AND BLOOD PH).

Other devices from Roche Diagnostics GmbH

See all devices from Roche Diagnostics GmbH →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)