gudid
Primary ID: 90CH.IN.004
Offset reamer handle - Dual Coupling (UDI 90CH.IN.004)
Manufactured by Incipio Devices SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Offset reamer handle - Dual Coupling - Primary ID 90CH.IN.004
Device Regulatory Overview
The Offset reamer handle - Dual Coupling (Model/Catalog Number: 90CH.IN.004) is a medical device manufactured by Incipio Devices SA. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90CH.IN.004
- Product Code / EMDN
- LXH
- Device Name
- 30 Offset Reamer Handle for hip arthroplasty
- Database Sync Date
- 2026-08-09 09:03:20
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 Offset reamer handle - Dual Coupling?
The registered manufacturer of record for Offset reamer handle - Dual Coupling is Incipio Devices SA.
What is the Primary UDI-DI identifier for Offset reamer handle - Dual Coupling?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90CH.IN.004.
What classification code is assigned to this device?
This device is registered under product classification code LXH.
Similar Classification Devices (LXH)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint