gudid
Primary ID: ACRL-2000
AccuRelief (UDI ACRL-2000)
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-2000
Device Regulatory Overview
The AccuRelief (Model/Catalog Number: ACRL-2000) is a medical device manufactured by Drive Devilbiss Healthcare. This product is indexed under FDA Product Code / Category Classification NUH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACRL-2000
- Product Code / EMDN
- NUH
- Device Name
- AccuRelief Single Channel TENS
- Database Sync Date
- 2026-08-09 09:00:33
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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-2000.
What classification code is assigned to this device?
This device is registered under product classification code NUH.
Similar Classification Devices (NUH)
Other Devices by Drive Devilbiss Healthcare
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