eudamed_udi
Primary ID: 08051881015739
VISIT LARGE (UDI 08051881015739)
Manufactured by CHINESPORT S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VISIT LARGE - Primary ID 08051881015739
Device Regulatory Overview
The VISIT LARGE (Model/Catalog Number: LV121A2WT) 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
- LV121A2WT
- Product Code / EMDN
- V080603
- Device Name
- VISIT
- Database Sync Date
- 2026-08-09 16:30:17
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 VISIT LARGE?
The registered manufacturer of record for VISIT LARGE is CHINESPORT S.P.A..
What is the Primary UDI-DI identifier for VISIT LARGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051881015739.
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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