eudamed_udi
Primary ID: 04052024054695
GNp Handgriff modular (UDI 04052024054695)
Manufactured by INTERCUS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GNp Handgriff modular - Primary ID 04052024054695
Device Regulatory Overview
The GNp Handgriff modular (Model/Catalog Number: 1133155) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification L99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1133155
- Product Code / EMDN
- L99
- Device Name
- Instrumente für GN Gleitnagelsystem (nicht invasiv)
- Database Sync Date
- 2026-08-09 17:15:33
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 GNp Handgriff modular?
The registered manufacturer of record for GNp Handgriff modular is INTERCUS GmbH.
What is the Primary UDI-DI identifier for GNp Handgriff modular?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024054695.
What classification code is assigned to this device?
This device is registered under product classification code L99.
Similar Classification Devices (L99)
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