GUDIDData
eudamed_udi Primary ID: 06934635740953

Extractor Φ4.5/Φ5.0 (UDI 06934635740953)

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 Extractor Φ4.5/Φ5.0 - Primary ID 06934635740953

Device Regulatory Overview

The Extractor Φ4.5/Φ5.0 (Model/Catalog Number: F16BB-PA00764) is a medical device manufactured by WUHAN MINDRAY SCIENTIFIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification L091101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
F16BB-PA00764
Product Code / EMDN
L091101
Device Name
Non-sterile Orthopedic Manual Surgical Instruments
Database Sync Date
2026-08-09 16:29:04

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Extractor Φ4.5/Φ5.0?

The registered manufacturer of record for Extractor Φ4.5/Φ5.0 is WUHAN MINDRAY SCIENTIFIC CO., LTD..

What is the Primary UDI-DI identifier for Extractor Φ4.5/Φ5.0?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06934635740953.

What classification code is assigned to this device?

This device is registered under product classification code L091101.

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