GUDIDData
gudid Primary ID: 823048

CODMAN (UDI 823048)

Manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CODMAN - Primary ID 823048

Device Regulatory Overview

The CODMAN (Model/Catalog Number: 823048) is a medical device manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION. This product is indexed under FDA Product Code / Category Classification JXG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
823048
Product Code / EMDN
JXG
Device Name
CODMAN Straight Connector
Database Sync Date
2026-08-09 09:31:12

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 CODMAN?

The registered manufacturer of record for CODMAN is INTEGRA LIFESCIENCES PRODUCTION CORPORATION.

What is the Primary UDI-DI identifier for CODMAN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 823048.

What classification code is assigned to this device?

This device is registered under product classification code JXG.

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