gudid
Primary ID: 1007106
NiTiBOND Nitinol/Titanium (UDI 1007106)
Manufactured by Heinz Kurz GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NiTiBOND Nitinol/Titanium - Primary ID 1007106
Device Regulatory Overview
The NiTiBOND Nitinol/Titanium (Model/Catalog Number: 1007106) is a medical device manufactured by Heinz Kurz GmbH. This product is indexed under FDA Product Code / Category Classification ETB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1007106
- Product Code / EMDN
- ETB
- Device Name
- Ossicular Prosthesis, partial
- Database Sync Date
- 2026-08-09 09:08:31
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of NiTiBOND Nitinol/Titanium?
The registered manufacturer of record for NiTiBOND Nitinol/Titanium is Heinz Kurz GmbH.
What is the Primary UDI-DI identifier for NiTiBOND Nitinol/Titanium?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1007106.
What classification code is assigned to this device?
This device is registered under product classification code ETB.
Similar Classification Devices (ETB)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint