GUDIDData
eudamed_udi Primary ID: 05210077006873

Πηχεοκαρπικός Nαρθηκας με Προσθαφαιρούμενη Λάμα, Αριστερό, Small (UDI 05210077006873)

Manufactured by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Πηχεοκαρπικός Nαρθηκας με Προσθαφαιρούμενη Λάμα, Αριστερό, Small - Primary ID 05210077006873

Device Regulatory Overview

The Πηχεοκαρπικός Nαρθηκας με Προσθαφαιρούμενη Λάμα, Αριστερό, Small (Model/Catalog Number: 103099) is a medical device manufactured by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
103099
Product Code / EMDN
Y060612
Device Name
Πηχεοκαρπικός Νάρθηκας με Προσθαφαιρούμενη Λάμα
Database Sync Date
2026-08-09 16:28:46

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 Πηχεοκαρπικός Nαρθηκας με Προσθαφαιρούμενη Λάμα, Αριστερό, Small?

The registered manufacturer of record for Πηχεοκαρπικός Nαρθηκας με Προσθαφαιρούμενη Λάμα, Αριστερό, Small is ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε..

What is the Primary UDI-DI identifier for Πηχεοκαρπικός Nαρθηκας με Προσθαφαιρούμενη Λάμα, Αριστερό, Small?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05210077006873.

What classification code is assigned to this device?

This device is registered under product classification code Y060612.

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