ΝΑΡΘΗΚΑΣ ΥΠΟΣΤΗΡΙΞΗΣ ΚΑΡΠΟΥ FOAM (UDI 05204914317352)
Manufactured by ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε.
Device Regulatory Overview
The ΝΑΡΘΗΚΑΣ ΥΠΟΣΤΗΡΙΞΗΣ ΚΑΡΠΟΥ FOAM (Model/Catalog Number: 0503) is a medical device manufactured by ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε.. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0503
- Product Code / EMDN
- Y060612
- Device Name
- ΝΑΡΘΗΚΑΣ ΥΠΟΣΤΗΡΙΞΗΣ ΚΑΡΠΟΥ FOAM / WRIST NARTHEX
- Database Sync Date
- 2026-08-09 16:29:09
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ΝΑΡΘΗΚΑΣ ΥΠΟΣΤΗΡΙΞΗΣ ΚΑΡΠΟΥ FOAM?
The registered manufacturer of record for ΝΑΡΘΗΚΑΣ ΥΠΟΣΤΗΡΙΞΗΣ ΚΑΡΠΟΥ FOAM is ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε..
What is the Primary UDI-DI identifier for ΝΑΡΘΗΚΑΣ ΥΠΟΣΤΗΡΙΞΗΣ ΚΑΡΠΟΥ FOAM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204914317352.
What classification code is assigned to this device?
This device is registered under product classification code Y060612.
Similar Classification Devices (Y060612)
Other Devices by ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε.
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