eudamed_udi
Primary ID: 04052024054572
GN Gleithammer gross (UDI 04052024054572)
Manufactured by INTERCUS GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GN Gleithammer gross - Primary ID 04052024054572
Device Regulatory Overview
The GN Gleithammer gross (Model/Catalog Number: 1133133) is a medical device manufactured by INTERCUS GmbH. This product is indexed under FDA Product Code / Category Classification L0903 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1133133
- Product Code / EMDN
- L0903
- Device Name
- Instrumente für GN Gleitnagelsystem (nicht invasiv)
- Database Sync Date
- 2026-08-09 18:11:13
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 GN Gleithammer gross?
The registered manufacturer of record for GN Gleithammer gross is INTERCUS GmbH.
What is the Primary UDI-DI identifier for GN Gleithammer gross?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04052024054572.
What classification code is assigned to this device?
This device is registered under product classification code L0903.
Similar Classification Devices (L0903)
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