GUDIDData
eudamed_udi Primary ID: 06926555496171

Bone Impactor (S) (UDI 06926555496171)

Manufactured by Shanghai REACH Medical Instrument Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bone Impactor (S) - Primary ID 06926555496171

Device Regulatory Overview

The Bone Impactor (S) (Model/Catalog Number: E06-R-0500-19) is a medical device manufactured by Shanghai REACH Medical Instrument Co., Ltd. This product is indexed under FDA Product Code / Category Classification L0999 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
E06-R-0500-19
Product Code / EMDN
L0999
Device Name
Orthopedic Instrument
Database Sync Date
2026-08-09 16:28:44

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 Bone Impactor (S)?

The registered manufacturer of record for Bone Impactor (S) is Shanghai REACH Medical Instrument Co., Ltd.

What is the Primary UDI-DI identifier for Bone Impactor (S)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06926555496171.

What classification code is assigned to this device?

This device is registered under product classification code L0999.

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