gudid
Primary ID: M004RA6201US0
RHYTHMIA HDx (UDI M004RA6201US0)
Manufactured by BOSTON SCIENTIFIC CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RHYTHMIA HDx - Primary ID M004RA6201US0
Device Regulatory Overview
The RHYTHMIA HDx (Model/Catalog Number: M004RA6201US0) is a medical device manufactured by BOSTON SCIENTIFIC CORPORATION. This product is indexed under FDA Product Code / Category Classification OAD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M004RA6201US0
- Product Code / EMDN
- OAD
- Device Name
- Ablation Connection Box (Maestro)
- Database Sync Date
- 2026-08-09 09:26:53
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 RHYTHMIA HDx?
The registered manufacturer of record for RHYTHMIA HDx is BOSTON SCIENTIFIC CORPORATION.
What is the Primary UDI-DI identifier for RHYTHMIA HDx?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M004RA6201US0.
What classification code is assigned to this device?
This device is registered under product classification code OAD.
Similar Classification Devices (OAD)
Other Devices by BOSTON SCIENTIFIC CORPORATION
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