eudamed_udi
Primary ID: 06936894760062
SHINVA (UDI 06936894760062)
Manufactured by Xinhua Surgical Instrument Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SHINVA - Primary ID 06936894760062
Device Regulatory Overview
The SHINVA (Model/Catalog Number: ZQ461RB) is a medical device manufactured by Xinhua Surgical Instrument Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification L0917 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZQ461RB
- Product Code / EMDN
- L0917
- Device Name
- Reusable Surgical Curettes/Elevators/Rongeurs/Chisels/Files/Bone levers
- Database Sync Date
- 2026-08-09 16:59:48
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 SHINVA?
The registered manufacturer of record for SHINVA is Xinhua Surgical Instrument Co.,Ltd..
What is the Primary UDI-DI identifier for SHINVA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936894760062.
What classification code is assigned to this device?
This device is registered under product classification code L0917.
Similar Classification Devices (L0917)
Other Devices by Xinhua Surgical Instrument Co.,Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint