GUDIDData
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eudamed_udi Primary ID: 08030413204667

CUFFIA ROTONDA AZZURRA CON ELASTICO - MOD. GIULIEIN - BOX DISPENSER - NON STERILE (UDI 08030413204667)

Manufactured by Mediberg S.r.l. Unipersonale

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CUFFIA ROTONDA AZZURRA CON ELASTICO - MOD. GIULIEIN - BOX DISPENSER - NON STERILE - Primary ID 08030413204667

Device Regulatory Overview

The CUFFIA ROTONDA AZZURRA CON ELASTICO - MOD. GIULIEIN - BOX DISPENSER - NON STERILE (Model/Catalog Number: 603009IB5NMD) is a medical device manufactured by Mediberg S.r.l. Unipersonale. This product is indexed under FDA Product Code / Category Classification T0207 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
603009IB5NMD
Product Code / EMDN
T0207
Device Name
ABBIGLIAMENTO MONOUSO NON STERILE
Database Sync Date
2026-08-09 16:30:01

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of CUFFIA ROTONDA AZZURRA CON ELASTICO - MOD. GIULIEIN - BOX DISPENSER - NON STERILE?

The registered manufacturer of record for CUFFIA ROTONDA AZZURRA CON ELASTICO - MOD. GIULIEIN - BOX DISPENSER - NON STERILE is Mediberg S.r.l. Unipersonale.

What is the Primary UDI-DI identifier for CUFFIA ROTONDA AZZURRA CON ELASTICO - MOD. GIULIEIN - BOX DISPENSER - NON STERILE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08030413204667.

What classification code is assigned to this device?

This device is registered under product classification code T0207.

Similar Classification Devices (T0207)

Other Devices by Mediberg S.r.l. Unipersonale

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