3D Μαξιλάρι Κατακλίσεων με Σφαιρίδια Σιλικόνης (UDI 05210077043649)
Manufactured by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.
Device Regulatory Overview
The 3D Μαξιλάρι Κατακλίσεων με Σφαιρίδια Σιλικόνης (Model/Catalog Number: 058.00273) is a medical device manufactured by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.. This product is indexed under FDA Product Code / Category Classification V08030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 058.00273
- Product Code / EMDN
- V08030102
- Device Name
- ΒΟΗΘΗΜΑΤΑ ΚΑΤΑΚΛΙΣΗΣ
- Database Sync Date
- 2026-08-09 17:59:54
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of 3D Μαξιλάρι Κατακλίσεων με Σφαιρίδια Σιλικόνης?
The registered manufacturer of record for 3D Μαξιλάρι Κατακλίσεων με Σφαιρίδια Σιλικόνης is ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε..
What is the Primary UDI-DI identifier for 3D Μαξιλάρι Κατακλίσεων με Σφαιρίδια Σιλικόνης?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05210077043649.
What classification code is assigned to this device?
This device is registered under product classification code V08030102.
Similar Classification Devices (V08030102)
Other Devices by ΧΡΙΣΤΟΦΟΡΟΣ ΚΥΦΙΔΗΣ ΚΑΙ ΣΙΑ Ε.Ε.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint