GUDIDData
gudid Primary ID: ACRL-0031

AccuRelief (UDI ACRL-0031)

Manufactured by Drive Devilbiss Healthcare

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AccuRelief - Primary ID ACRL-0031

Device Regulatory Overview

The AccuRelief (Model/Catalog Number: ACRL-0031) is a medical device manufactured by Drive Devilbiss Healthcare. This product is indexed under FDA Product Code / Category Classification GXY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ACRL-0031
Product Code / EMDN
GXY
Device Name
AccuRelief TENS Supply Kit LG
Database Sync Date
2026-08-09 09:00:33

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of AccuRelief?

The registered manufacturer of record for AccuRelief is Drive Devilbiss Healthcare.

What is the Primary UDI-DI identifier for AccuRelief?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ACRL-0031.

What classification code is assigned to this device?

This device is registered under product classification code GXY.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint