gudid
Primary ID: 823056
CODMAN (UDI 823056)
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 823056
Device Regulatory Overview
The CODMAN (Model/Catalog Number: 823056) 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
- 823056
- Product Code / EMDN
- JXG
- Device Name
- CODMAN Tube Passer
- 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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Get API Token Access ($49/mo)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 823056.
What classification code is assigned to this device?
This device is registered under product classification code JXG.
Similar Classification Devices (JXG)
Other Devices by INTEGRA LIFESCIENCES PRODUCTION CORPORATION
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