eudamed_udi
Primary ID: 28058945153868
Evo Specific SPA (UDI 28058945153868)
Manufactured by ABD SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Evo Specific SPA - Primary ID 28058945153868
Device Regulatory Overview
The Evo Specific SPA (Model/Catalog Number: 1N3300 D205) is a medical device manufactured by ABD SRL. This product is indexed under FDA Product Code / Category Classification W0102019099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1N3300 D205
- Product Code / EMDN
- W0102019099
- Device Name
- Allergy SPA Recombinants - Allergia SPA Ricombinanti
- Database Sync Date
- 2026-08-09 16:28:57
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 Evo Specific SPA?
The registered manufacturer of record for Evo Specific SPA is ABD SRL.
What is the Primary UDI-DI identifier for Evo Specific SPA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28058945153868.
What classification code is assigned to this device?
This device is registered under product classification code W0102019099.
Similar Classification Devices (W0102019099)
Other Devices by ABD SRL
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