GUDIDData
eudamed_udi Primary ID: 04250203224437

Trachealkanüle PRIMEDIPHON®, Gr.11, L = 87 mm (UDI 04250203224437)

Manufactured by Primed Halberstadt Medizintechnik GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Trachealkanüle PRIMEDIPHON®, Gr.11, L = 87 mm - Primary ID 04250203224437

Device Regulatory Overview

The Trachealkanüle PRIMEDIPHON®, Gr.11, L = 87 mm (Model/Catalog Number: 200713) is a medical device manufactured by Primed Halberstadt Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification R0105020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
200713
Product Code / EMDN
R0105020101
Device Name
Primedistom
Database Sync Date
2026-08-09 16:47:21

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 Trachealkanüle PRIMEDIPHON®, Gr.11, L = 87 mm?

The registered manufacturer of record for Trachealkanüle PRIMEDIPHON®, Gr.11, L = 87 mm is Primed Halberstadt Medizintechnik GmbH.

What is the Primary UDI-DI identifier for Trachealkanüle PRIMEDIPHON®, Gr.11, L = 87 mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250203224437.

What classification code is assigned to this device?

This device is registered under product classification code R0105020101.

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