eudamed_udi
Primary ID: 08033140280843
BENDA ORLATA AURICOLARE 5m x 2cm pz 1 (UDI 08033140280843)
Manufactured by Previs S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BENDA ORLATA AURICOLARE 5m x 2cm pz 1 - Primary ID 08033140280843
Device Regulatory Overview
The BENDA ORLATA AURICOLARE 5m x 2cm pz 1 (Model/Catalog Number: AUR0500210PR) is a medical device manufactured by Previs S.r.l.. This product is indexed under FDA Product Code / Category Classification M030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AUR0500210PR
- Product Code / EMDN
- M030101
- Device Name
- BENDA DI GARZA ORLATA
- Database Sync Date
- 2026-08-09 16:29:22
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 ORLATA AURICOLARE 5m x 2cm pz 1?
The registered manufacturer of record for BENDA ORLATA AURICOLARE 5m x 2cm pz 1 is Previs S.r.l..
What is the Primary UDI-DI identifier for BENDA ORLATA AURICOLARE 5m x 2cm pz 1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033140280843.
What classification code is assigned to this device?
This device is registered under product classification code M030101.
Similar Classification Devices (M030101)
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