eudamed_udi
Primary ID: 05903240791224
VELOTEX (UDI 05903240791224)
Manufactured by Ferita Tytus Biegański
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VELOTEX - Primary ID 05903240791224
Device Regulatory Overview
The VELOTEX (Model/Catalog Number: VELOTEX 1/TX-SO-0110 (10m)) is a medical device manufactured by Ferita Tytus Biegański. This product is indexed under FDA Product Code / Category Classification M030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VELOTEX 1/TX-SO-0110 (10m)
- Product Code / EMDN
- M030499
- Device Name
- siatka opatrunkowa VELOTEX
- Database Sync Date
- 2026-08-09 16:28:47
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 VELOTEX?
The registered manufacturer of record for VELOTEX is Ferita Tytus Biegański.
What is the Primary UDI-DI identifier for VELOTEX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903240791224.
What classification code is assigned to this device?
This device is registered under product classification code M030499.
Similar Classification Devices (M030499)
Other Devices by Ferita Tytus Biegański
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