eudamed_udi
Primary ID: 08057971310067
DIA XL (UDI 08057971310067)
Manufactured by Quality Invents srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DIA XL - Primary ID 08057971310067
Device Regulatory Overview
The DIA XL (Model/Catalog Number: Q-1010-26) is a medical device manufactured by Quality Invents srl. This product is indexed under FDA Product Code / Category Classification W02079099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Q-1010-26
- Product Code / EMDN
- W02079099
- Device Name
- Reverse osmosis deionizer
- Database Sync Date
- 2026-08-09 18:59:54
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 DIA XL?
The registered manufacturer of record for DIA XL is Quality Invents srl.
What is the Primary UDI-DI identifier for DIA XL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057971310067.
What classification code is assigned to this device?
This device is registered under product classification code W02079099.
Similar Classification Devices (W02079099)
Other Devices by Quality Invents srl
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