gudid
Primary ID: Regular Pack
Accusil Light Body (UDI Regular Pack)
Manufactured by PREVEST DENPRO LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Accusil Light Body - Primary ID Regular Pack
Device Regulatory Overview
The Accusil Light Body (Model/Catalog Number: Regular Pack) is a medical device manufactured by PREVEST DENPRO LIMITED. This product is indexed under FDA Product Code / Category Classification ELW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Regular Pack
- Product Code / EMDN
- ELW
- Device Name
- Database Sync Date
- 2026-08-09 09:01:11
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 Accusil Light Body?
The registered manufacturer of record for Accusil Light Body is PREVEST DENPRO LIMITED.
What is the Primary UDI-DI identifier for Accusil Light Body?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Regular Pack.
What classification code is assigned to this device?
This device is registered under product classification code ELW.
Similar Classification Devices (ELW)
Other Devices by PREVEST DENPRO LIMITED
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