GUDIDData
eudamed_udi Primary ID: 05210077043236

ΝΑΡΘΗΚΑΣ ΟΜΣΣ Ή ΘΜΣΣ ΜΕ ΚΟΡΔΟΝΙ ΣΥΜΠΙΕΣΗΣ (UDI 05210077043236)

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 ΝΑΡΘΗΚΑΣ ΟΜΣΣ Ή ΘΜΣΣ ΜΕ ΚΟΡΔΟΝΙ ΣΥΜΠΙΕΣΗΣ - Primary ID 05210077043236

Device Regulatory Overview

The ΝΑΡΘΗΚΑΣ ΟΜΣΣ Ή ΘΜΣΣ ΜΕ ΚΟΡΔΟΝΙ ΣΥΜΠΙΕΣΗΣ (Model/Catalog Number: 058.00119) is a medical device manufactured by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.. This product is indexed under FDA Product Code / Category Classification Y060309 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
058.00119
Product Code / EMDN
Y060309
Device Name
ΚΟΡΜΙΚΟΙ ΚΗΔΕΜΟΝΕΣ
Database Sync Date
2026-08-09 16:59:12

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 ΝΑΡΘΗΚΑΣ ΟΜΣΣ Ή ΘΜΣΣ ΜΕ ΚΟΡΔΟΝΙ ΣΥΜΠΙΕΣΗΣ?

The registered manufacturer of record for ΝΑΡΘΗΚΑΣ ΟΜΣΣ Ή ΘΜΣΣ ΜΕ ΚΟΡΔΟΝΙ ΣΥΜΠΙΕΣΗΣ is ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε..

What is the Primary UDI-DI identifier for ΝΑΡΘΗΚΑΣ ΟΜΣΣ Ή ΘΜΣΣ ΜΕ ΚΟΡΔΟΝΙ ΣΥΜΠΙΕΣΗΣ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05210077043236.

What classification code is assigned to this device?

This device is registered under product classification code Y060309.

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