gudid
Primary ID: 9005-00-030
NA (UDI 9005-00-030)
Manufactured by DEPUY INTERNATIONAL LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 9005-00-030
Device Regulatory Overview
The NA (Model/Catalog Number: 9005-00-030) is a medical device manufactured by DEPUY INTERNATIONAL LTD. This product is indexed under FDA Product Code / Category Classification LYS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9005-00-030
- Product Code / EMDN
- LYS
- Device Name
- NOVIOMAGUS BONE MILL - Housing
- Database Sync Date
- 2026-08-09 09:31:05
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 NA?
The registered manufacturer of record for NA is DEPUY INTERNATIONAL LTD.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9005-00-030.
What classification code is assigned to this device?
This device is registered under product classification code LYS.
Similar Classification Devices (LYS)
Other Devices by DEPUY INTERNATIONAL LTD
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