Lagerungssieb, für TWISTER-I-Schrauben und Knochenklammern, Kunststoff, komplett (UDI 04052024059096)
Manufactured by INTERCUS GmbH
Device Regulatory Overview
The Lagerungssieb, für TWISTER-I-Schrauben und Knochenklammern, Kunststoff, komplett (Model/Catalog Number: 750.108828) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification V0480 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 750.108828
- Product Code / EMDN
- V0480
- Device Name
- Lagerungssysteme für Implantate und Instrumente (Kunststoff)
- Database Sync Date
- 2026-08-09 18:50:35
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 Lagerungssieb, für TWISTER-I-Schrauben und Knochenklammern, Kunststoff, komplett?
The registered manufacturer of record for Lagerungssieb, für TWISTER-I-Schrauben und Knochenklammern, Kunststoff, komplett is INTERCUS GmbH.
What is the Primary UDI-DI identifier for Lagerungssieb, für TWISTER-I-Schrauben und Knochenklammern, Kunststoff, komplett?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024059096.
What classification code is assigned to this device?
This device is registered under product classification code V0480.
Similar Classification Devices (V0480)
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