ΚΟΜΟΔΙΝΟ ΝΟΣΗΛΕΙΑΣ 15001 (UDI 05200143610271)
Manufactured by ΚΕΠΑ ΑΝΩΝΥΜΗ ΒΙΟΤΕΧΝΙΚΗ ΕΜΠΟΡΙΚΗ ΕΤΑΙΡΕΙΑ
Device Regulatory Overview
The ΚΟΜΟΔΙΝΟ ΝΟΣΗΛΕΙΑΣ 15001 (Model/Catalog Number: 15001) is a medical device manufactured by ΚΕΠΑ ΑΝΩΝΥΜΗ ΒΙΟΤΕΧΝΙΚΗ ΕΜΠΟΡΙΚΗ ΕΤΑΙΡΕΙΑ. This product is indexed under FDA Product Code / Category Classification Y1803 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 15001
- Product Code / EMDN
- Y1803
- Device Name
- ΚΟΜΟΔΙΝΟ ΝΟΣΗΛΕΙΑΣ
- Database Sync Date
- 2026-08-09 16:51:58
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 ΚΟΜΟΔΙΝΟ ΝΟΣΗΛΕΙΑΣ 15001?
The registered manufacturer of record for ΚΟΜΟΔΙΝΟ ΝΟΣΗΛΕΙΑΣ 15001 is ΚΕΠΑ ΑΝΩΝΥΜΗ ΒΙΟΤΕΧΝΙΚΗ ΕΜΠΟΡΙΚΗ ΕΤΑΙΡΕΙΑ.
What is the Primary UDI-DI identifier for ΚΟΜΟΔΙΝΟ ΝΟΣΗΛΕΙΑΣ 15001?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05200143610271.
What classification code is assigned to this device?
This device is registered under product classification code Y1803.
Similar Classification Devices (Y1803)
Other Devices by ΚΕΠΑ ΑΝΩΝΥΜΗ ΒΙΟΤΕΧΝΙΚΗ ΕΜΠΟΡΙΚΗ ΕΤΑΙΡΕΙΑ
Programmatic Export
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