GUDIDData
eudamed_udi Primary ID: 05213013380082

OLSETRF05 (UDI 05213013380082)

Manufactured by ΜΕΝΤΙΓΟΥΕΙ ΕΙΣΑΓΩΓΗ & ΕΜΠΟΡΙΑ ΙΑΤΡΙΚΩΝ ΝΟΣΟΚΟΜΕΙΟΑΚΩΝ ΜΗΧΑΝΗΜΑΤΩΝ Μ. Ε.Π.Ε.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OLSETRF05 - Primary ID 05213013380082

Device Regulatory Overview

The OLSETRF05 (Model/Catalog Number: OLSETRF05) is a medical device manufactured by ΜΕΝΤΙΓΟΥΕΙ ΕΙΣΑΓΩΓΗ & ΕΜΠΟΡΙΑ ΙΑΤΡΙΚΩΝ ΝΟΣΟΚΟΜΕΙΟΑΚΩΝ ΜΗΧΑΝΗΜΑΤΩΝ Μ. Ε.Π.Ε.. This product is indexed under FDA Product Code / Category Classification K0201010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
OLSETRF05
Product Code / EMDN
K0201010301
Device Name
ΣΕΤ ΗΛΕΚΤΡΟΔΙΩΝ ΡΑΔΙΟΚΥΜΑΤΩΝ
Database Sync Date
2026-08-09 16:29:02

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 OLSETRF05?

The registered manufacturer of record for OLSETRF05 is ΜΕΝΤΙΓΟΥΕΙ ΕΙΣΑΓΩΓΗ & ΕΜΠΟΡΙΑ ΙΑΤΡΙΚΩΝ ΝΟΣΟΚΟΜΕΙΟΑΚΩΝ ΜΗΧΑΝΗΜΑΤΩΝ Μ. Ε.Π.Ε..

What is the Primary UDI-DI identifier for OLSETRF05?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213013380082.

What classification code is assigned to this device?

This device is registered under product classification code K0201010301.

Similar Classification Devices (K0201010301)

Other Devices by ΜΕΝΤΙΓΟΥΕΙ ΕΙΣΑΓΩΓΗ & ΕΜΠΟΡΙΑ ΙΑΤΡΙΚΩΝ ΝΟΣΟΚΟΜΕΙΟΑΚΩΝ ΜΗΧΑΝΗΜΑΤΩΝ Μ. Ε.Π.Ε.

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