GUDIDData
eudamed_udi Primary ID: 05210077043595

Ειδική Καρέκλα Ανύψωσης (UDI 05210077043595)

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 Ειδική Καρέκλα Ανύψωσης - Primary ID 05210077043595

Device Regulatory Overview

The Ειδική Καρέκλα Ανύψωσης (Model/Catalog Number: 058.00041) is a medical device manufactured by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.. This product is indexed under FDA Product Code / Category Classification V0805030101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
058.00041
Product Code / EMDN
V0805030101
Device Name
Συσκευές Ανύψωσης Ατόμων
Database Sync Date
2026-08-09 18:10:01

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 Ειδική Καρέκλα Ανύψωσης?

The registered manufacturer of record for Ειδική Καρέκλα Ανύψωσης is ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε..

What is the Primary UDI-DI identifier for Ειδική Καρέκλα Ανύψωσης?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05210077043595.

What classification code is assigned to this device?

This device is registered under product classification code V0805030101.

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