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AccuRelief ACRL-0052

by Drive Devilbiss Healthcare United States GUDID

Product code GXY

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00023601200525 UDI-DIDate7 Oct 2025ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 23 Oct 2026)

Specification

GUDID · synced 23 Oct 2026

Trade Name
AccuRelief
Generic Name
Transcutaneous electrical stimulation electrode, single-use
Model / Reference
ACRL-0052
Primary DI / UDI-DI
00023601200525
FDA Product Code
GXY
GMDN Term
Transcutaneous electrical stimulation electrode, single-use
Device Class
Class II
Regulation Number
882.1320
Commercial Distribution
In Commercial Distribution

Other devices from Drive Devilbiss Healthcare

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Properties & raw data

Show properties, registry sources and raw records
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date
Other properties (11)
  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No

Sources (1)

  • FDA UDI f2a28eef-cd2d-425c-9440-5caeb9e23501 34 fields · synced 23 Oct 2026