eudamed_udi
Primary ID: 05940741460341
IZIS Orvosi kevert vatta 100 g-os (UDI 05940741460341)
Manufactured by EUROCOSMETIC s.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IZIS Orvosi kevert vatta 100 g-os - Primary ID 05940741460341
Device Regulatory Overview
The IZIS Orvosi kevert vatta 100 g-os (Model/Catalog Number: IZIS100100K) is a medical device manufactured by EUROCOSMETIC s.r.l.. This product is indexed under FDA Product Code / Category Classification M010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IZIS100100K
- Product Code / EMDN
- M010101
- Device Name
- VATA HIDROFILA DE UZ MEDICINAL
- Database Sync Date
- 2026-08-09 16:29:56
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 IZIS Orvosi kevert vatta 100 g-os?
The registered manufacturer of record for IZIS Orvosi kevert vatta 100 g-os is EUROCOSMETIC s.r.l..
What is the Primary UDI-DI identifier for IZIS Orvosi kevert vatta 100 g-os?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940741460341.
What classification code is assigned to this device?
This device is registered under product classification code M010101.
Similar Classification Devices (M010101)
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