gudid
Primary ID: M001711250
WALLSTENT RP Endoprosthesis (UDI M001711250)
Manufactured by BOSTON SCIENTIFIC CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WALLSTENT RP Endoprosthesis - Primary ID M001711250
Device Regulatory Overview
The WALLSTENT RP Endoprosthesis (Model/Catalog Number: M001711250) 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
- M001711250
- Product Code / EMDN
- JCT
- Device Name
- Self-Expanding Stent
- Database Sync Date
- 2026-08-09 09:41:08
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 WALLSTENT RP Endoprosthesis?
The registered manufacturer of record for WALLSTENT RP Endoprosthesis is BOSTON SCIENTIFIC CORPORATION.
What is the Primary UDI-DI identifier for WALLSTENT RP Endoprosthesis?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M001711250.
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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