GUDIDData
eudamed_udi Primary ID: 08720261240664

Lichtgeleider ø3mm x 207mm (UDI 08720261240664)

Manufactured by Medex Instrumenten Service

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lichtgeleider ø3mm x 207mm - Primary ID 08720261240664

Device Regulatory Overview

The Lichtgeleider ø3mm x 207mm (Model/Catalog Number: ME30-30-207) is a medical device manufactured by Medex Instrumenten Service. This product is indexed under FDA Product Code / Category Classification L149099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ME30-30-207
Product Code / EMDN
L149099
Device Name
ENT INSTRUMENTS, REUSABLE - OTHER
Database Sync Date
2026-08-09 16:58:18

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 Lichtgeleider ø3mm x 207mm?

The registered manufacturer of record for Lichtgeleider ø3mm x 207mm is Medex Instrumenten Service.

What is the Primary UDI-DI identifier for Lichtgeleider ø3mm x 207mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720261240664.

What classification code is assigned to this device?

This device is registered under product classification code L149099.

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