eudamed_udi
Primary ID: 08051881019966
STRUZZO RC (UDI 08051881019966)
Manufactured by CHINESPORT S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STRUZZO RC - Primary ID 08051881019966
Device Regulatory Overview
The STRUZZO RC (Model/Catalog Number: AV3521B3342C) is a medical device manufactured by CHINESPORT S.P.A.. This product is indexed under FDA Product Code / Category Classification V0805030101,V0805030102,Y050202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AV3521B3342C
- Product Code / EMDN
- V0805030101,V0805030102,Y050202
- Device Name
- AV3 STANDING FRAMES
- Database Sync Date
- 2026-08-09 17:24:01
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 STRUZZO RC?
The registered manufacturer of record for STRUZZO RC is CHINESPORT S.P.A..
What is the Primary UDI-DI identifier for STRUZZO RC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051881019966.
What classification code is assigned to this device?
This device is registered under product classification code V0805030101,V0805030102,Y050202.
Similar Classification Devices (V0805030101,V0805030102,Y050202)
Other Devices by CHINESPORT S.P.A.
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