eudamed_udi
Primary ID: 08591846933185
MGF Variant, size 3XL, black (UDI 08591846933185)
Manufactured by LIPOELASTIC a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MGF Variant, size 3XL, black - Primary ID 08591846933185
Device Regulatory Overview
The MGF Variant, size 3XL, black (Model/Catalog Number: LIPO-MGF00V00R-B-3XL) is a medical device manufactured by LIPOELASTIC a.s.. This product is indexed under FDA Product Code / Category Classification M030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LIPO-MGF00V00R-B-3XL
- Product Code / EMDN
- M030499
- Device Name
- R/MGF Variant
- Database Sync Date
- 2026-08-09 16:30:10
Full Regulatory Attributes
🔒 Token Gated
{
"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 MGF Variant, size 3XL, black?
The registered manufacturer of record for MGF Variant, size 3XL, black is LIPOELASTIC a.s..
What is the Primary UDI-DI identifier for MGF Variant, size 3XL, black?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08591846933185.
What classification code is assigned to this device?
This device is registered under product classification code M030499.
Similar Classification Devices (M030499)
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