eudamed_udi
Primary ID: 08052219480014
ARES (UDI 08052219480014)
Manufactured by GNG S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARES - Primary ID 08052219480014
Device Regulatory Overview
The ARES (Model/Catalog Number: ARES) is a medical device manufactured by GNG S.R.L.. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ARES
- Product Code / EMDN
- Z12069099
- Device Name
- AR-1X300W-MF Dispositivo di trasmissione energetica per diatermia / Energy transmission device for diathermy
- Database Sync Date
- 2026-08-09 16:28:51
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 ARES?
The registered manufacturer of record for ARES is GNG S.R.L..
What is the Primary UDI-DI identifier for ARES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08052219480014.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
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