gudid
Primary ID: 1015075
Ventilation Tube Trocar Titanium (UDI 1015075)
Manufactured by Heinz Kurz GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ventilation Tube Trocar Titanium - Primary ID 1015075
Device Regulatory Overview
The Ventilation Tube Trocar Titanium (Model/Catalog Number: 1015075) is a medical device manufactured by Heinz Kurz GmbH. This product is indexed under FDA Product Code / Category Classification ETD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1015075
- Product Code / EMDN
- ETD
- Device Name
- Middle ear implantable mould
- Database Sync Date
- 2026-08-09 09:08:30
Full Regulatory Attributes
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{
"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 Ventilation Tube Trocar Titanium?
The registered manufacturer of record for Ventilation Tube Trocar Titanium is Heinz Kurz GmbH.
What is the Primary UDI-DI identifier for Ventilation Tube Trocar Titanium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1015075.
What classification code is assigned to this device?
This device is registered under product classification code ETD.
Similar Classification Devices (ETD)
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