GUDIDData
eudamed_udi Primary ID: 00840277117571

Chen Diaphyseal Fracture Reduction Clamp (UDI 00840277117571)

Manufactured by Innomed, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Chen Diaphyseal Fracture Reduction Clamp - Primary ID 00840277117571

Device Regulatory Overview

The Chen Diaphyseal Fracture Reduction Clamp (Model/Catalog Number: 1808) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L091399 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1753-2024 View Full Alert →

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup...

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Technical Specifications

Model Number
1808
Product Code / EMDN
L091399
Device Name
Forceps
Database Sync Date
2026-08-09 16:29:29

Full Regulatory Attributes

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{
    "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 Chen Diaphyseal Fracture Reduction Clamp?

The registered manufacturer of record for Chen Diaphyseal Fracture Reduction Clamp is Innomed, Inc..

What is the Primary UDI-DI identifier for Chen Diaphyseal Fracture Reduction Clamp?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277117571.

What classification code is assigned to this device?

This device is registered under product classification code L091399.

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