ΣΛΙΠ ΚΗΛΗΣ (UDI 05204914324886)
Manufactured by ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε.
Device Regulatory Overview
The ΣΛΙΠ ΚΗΛΗΣ (Model/Catalog Number: 0343) 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 M030402010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0343
- Product Code / EMDN
- M030402010101
- Device Name
- ΣΛΙΠ ΚΗΛΗΣ / HERNIA UNDERWEAR
- Database Sync Date
- 2026-08-09 16:29:04
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 ΣΛΙΠ ΚΗΛΗΣ?
The registered manufacturer of record for ΣΛΙΠ ΚΗΛΗΣ is ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε..
What is the Primary UDI-DI identifier for ΣΛΙΠ ΚΗΛΗΣ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204914324886.
What classification code is assigned to this device?
This device is registered under product classification code M030402010101.
Similar Classification Devices (M030402010101)
Other Devices by ΑΝΑΤΟΜΙΚ ΧΕΛΠ ΑΝΩΝΥΜΗ ΕΤΑΙΡΙΑ ΕΜΠΟΡΙΑΣ ΚΑΙ ΚΑΤΑΣΚΕΥΗΣ ΟΡΘΟΠΕΔΙΚΩΝ ΕΙΔΩΝ Α.Ε.
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