eudamed_udi
Primary ID: 08051881007123
STRUZZO RCR (UDI 08051881007123)
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 RCR - Primary ID 08051881007123
Device Regulatory Overview
The STRUZZO RCR (Model/Catalog Number: AV3421B3452C) 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
- AV3421B3452C
- Product Code / EMDN
- V0805030101,V0805030102,Y050202
- Device Name
- AV3 STANDING FRAMES
- Database Sync Date
- 2026-08-09 16:47:04
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 RCR?
The registered manufacturer of record for STRUZZO RCR is CHINESPORT S.P.A..
What is the Primary UDI-DI identifier for STRUZZO RCR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051881007123.
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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