eudamed_udi
Primary ID: 08053848210027
Painaway (UDI 08053848210027)
Manufactured by ITALRES SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Painaway - Primary ID 08053848210027
Device Regulatory Overview
The Painaway (Model/Catalog Number: 30DM) is a medical device manufactured by ITALRES SRL. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30DM
- Product Code / EMDN
- Z12062899
- Device Name
- Paingone One
- Database Sync Date
- 2026-08-09 17:33:24
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 Painaway?
The registered manufacturer of record for Painaway is ITALRES SRL.
What is the Primary UDI-DI identifier for Painaway?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053848210027.
What classification code is assigned to this device?
This device is registered under product classification code Z12062899.
Similar Classification Devices (Z12062899)
Other Devices by ITALRES SRL
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