eudamed_udi
Primary ID: 08051881018228
TEST UROGYN (UDI 08051881018228)
Manufactured by CHINESPORT S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TEST UROGYN - Primary ID 08051881018228
Device Regulatory Overview
The TEST UROGYN (Model/Catalog Number: LE151D2WE) is a medical device manufactured by CHINESPORT S.P.A.. This product is indexed under FDA Product Code / Category Classification V080603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LE151D2WE
- Product Code / EMDN
- V080603
- Device Name
- TEST
- Database Sync Date
- 2026-08-09 16:29:36
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 TEST UROGYN?
The registered manufacturer of record for TEST UROGYN is CHINESPORT S.P.A..
What is the Primary UDI-DI identifier for TEST UROGYN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051881018228.
What classification code is assigned to this device?
This device is registered under product classification code V080603.
Similar Classification Devices (V080603)
Other Devices by CHINESPORT S.P.A.
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