gudid
Primary ID: 49341
Cardioblate (UDI 49341)
Manufactured by MEDTRONIC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cardioblate - Primary ID 49341
Device Regulatory Overview
The Cardioblate (Model/Catalog Number: 49341) is a medical device manufactured by MEDTRONIC, INC.. This product is indexed under FDA Product Code / Category Classification OCL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 49341
- Product Code / EMDN
- OCL
- Device Name
- CLAMP 49341 CARDIOBLATE LP FT
- Database Sync Date
- 2026-08-09 09:18:29
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Cardioblate?
The registered manufacturer of record for Cardioblate is MEDTRONIC, INC..
What is the Primary UDI-DI identifier for Cardioblate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 49341.
What classification code is assigned to this device?
This device is registered under product classification code OCL.
Similar Classification Devices (OCL)
Other Devices by MEDTRONIC, INC.
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