gudid
Primary ID: M00576430
Ultraflex Tracheobronchial (UDI M00576430)
Manufactured by BOSTON SCIENTIFIC CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultraflex Tracheobronchial - Primary ID M00576430
Device Regulatory Overview
The Ultraflex Tracheobronchial (Model/Catalog Number: M00576430) is a medical device manufactured by BOSTON SCIENTIFIC CORPORATION. This product is indexed under FDA Product Code / Category Classification JCT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M00576430
- Product Code / EMDN
- JCT
- Device Name
- Proximal Release Stent System
- Database Sync Date
- 2026-08-09 09:26:56
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 Ultraflex Tracheobronchial?
The registered manufacturer of record for Ultraflex Tracheobronchial is BOSTON SCIENTIFIC CORPORATION.
What is the Primary UDI-DI identifier for Ultraflex Tracheobronchial?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M00576430.
What classification code is assigned to this device?
This device is registered under product classification code JCT.
Similar Classification Devices (JCT)
Other Devices by BOSTON SCIENTIFIC CORPORATION
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