eudamed_udi
Primary ID: 06934635737458
Wire Guide (UDI 06934635737458)
Manufactured by WUHAN MINDRAY SCIENTIFIC CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wire Guide - Primary ID 06934635737458
Device Regulatory Overview
The Wire Guide (Model/Catalog Number: F16BB-PA00055) is a medical device manufactured by WUHAN MINDRAY SCIENTIFIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification L098099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F16BB-PA00055
- Product Code / EMDN
- L098099
- Device Name
- Non-sterile Orthopedic Manual Surgical Instruments
- Database Sync Date
- 2026-08-09 16:28:47
Full Regulatory Attributes
🔒 Token Gated
{
"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 Wire Guide?
The registered manufacturer of record for Wire Guide is WUHAN MINDRAY SCIENTIFIC CO., LTD..
What is the Primary UDI-DI identifier for Wire Guide?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06934635737458.
What classification code is assigned to this device?
This device is registered under product classification code L098099.
Similar Classification Devices (L098099)
Other Devices by WUHAN MINDRAY SCIENTIFIC CO., LTD.
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