eudamed_udi
Primary ID: D-CZMF000037078FHV30A3VHJ
MAJOR SUPER LUX VITA (UDI D-CZMF000037078FHV30A3VHJ)
Manufactured by MAJOR CZ s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAJOR SUPER LUX VITA - Primary ID D-CZMF000037078FHV30A3VHJ
Device Regulatory Overview
The MAJOR SUPER LUX VITA (Model/Catalog Number: N/A) is a medical device manufactured by MAJOR CZ s.r.o.. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- Q010299
- Device Name
- MAJOR SUPER LUX
- Database Sync Date
- 2026-08-09 16:28:53
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 MAJOR SUPER LUX VITA?
The registered manufacturer of record for MAJOR SUPER LUX VITA is MAJOR CZ s.r.o..
What is the Primary UDI-DI identifier for MAJOR SUPER LUX VITA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-CZMF000037078FHV30A3VHJ.
What classification code is assigned to this device?
This device is registered under product classification code Q010299.
Similar Classification Devices (Q010299)
Other Devices by MAJOR CZ s.r.o.
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