eudamed_udi
Primary ID: 08055271933429
20.22 - MATERASSO GONFIABILE A BOLLE (UDI 08055271933429)
Manufactured by VASSILLI S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 20.22 - MATERASSO GONFIABILE A BOLLE - Primary ID 08055271933429
Device Regulatory Overview
The 20.22 - MATERASSO GONFIABILE A BOLLE (Model/Catalog Number: 20.22) is a medical device manufactured by VASSILLI S.R.L.. This product is indexed under FDA Product Code / Category Classification V080701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20.22
- Product Code / EMDN
- V080701
- Device Name
- Materassi gonfiabili.
- Database Sync Date
- 2026-08-09 16:28:53
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 20.22 - MATERASSO GONFIABILE A BOLLE?
The registered manufacturer of record for 20.22 - MATERASSO GONFIABILE A BOLLE is VASSILLI S.R.L..
What is the Primary UDI-DI identifier for 20.22 - MATERASSO GONFIABILE A BOLLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055271933429.
What classification code is assigned to this device?
This device is registered under product classification code V080701.
Similar Classification Devices (V080701)
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