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Technomed Europe CS-ARR2115

by Technomed Engineering B.V.

Technomed Europe CS-ARR2115 is a Class II device made by Technomed Engineering B.V., listed in FDA GUDID since 8 Jul 2026 (UDI-DI 08720791378332), 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 Number08720791378332 UDI-DI Date8 Jul 2026ListedStatusListed 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  • Withdrawn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
Technomed Europe
Generic name
Analytical scalp electrode, single-use
Model / reference
CS-ARR2115
Primary DI / UDI-DI
08720791378332
FDA product code
GXY
GMDN term
Analytical scalp electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

Other devices from Technomed Engineering B.V.

See all devices from Technomed Engineering B.V. →

Properties

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