eudamed_udi
Primary ID: 05711014700231
Belly (UDI 05711014700231)
Manufactured by Levabo ApS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Belly - Primary ID 05711014700231
Device Regulatory Overview
The Belly (Model/Catalog Number: 70023) is a medical device manufactured by Levabo ApS. This product is indexed under FDA Product Code / Category Classification V08030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 70023
- Product Code / EMDN
- V08030102
- Device Name
- Multi Small
- Database Sync Date
- 2026-08-09 16:28:50
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 Belly?
The registered manufacturer of record for Belly is Levabo ApS.
What is the Primary UDI-DI identifier for Belly?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05711014700231.
What classification code is assigned to this device?
This device is registered under product classification code V08030102.
Similar Classification Devices (V08030102)
Other Devices by Levabo ApS
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