eudamed_udi
Primary ID: 05999571422241
Benda previmedical nuda 10pz 5mx12cm (UDI 05999571422241)
Manufactured by Medinovitas Kft
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Benda previmedical nuda 10pz 5mx12cm - Primary ID 05999571422241
Device Regulatory Overview
The Benda previmedical nuda 10pz 5mx12cm (Model/Catalog Number: MED050122) is a medical device manufactured by Medinovitas Kft. This product is indexed under FDA Product Code / Category Classification M0304010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MED050122
- Product Code / EMDN
- M0304010103
- Device Name
- Benda elastica Previforte
- Database Sync Date
- 2026-08-09 16:46:10
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 Benda previmedical nuda 10pz 5mx12cm?
The registered manufacturer of record for Benda previmedical nuda 10pz 5mx12cm is Medinovitas Kft.
What is the Primary UDI-DI identifier for Benda previmedical nuda 10pz 5mx12cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05999571422241.
What classification code is assigned to this device?
This device is registered under product classification code M0304010103.
Similar Classification Devices (M0304010103)
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