Maestro 3000 RF Cardiac Ablation Pod 100 (UDI M00421860TR0)
Manufactured by BOSTON SCIENTIFIC CORPORATION
Device Regulatory Overview
The Maestro 3000 RF Cardiac Ablation Pod 100 (Model/Catalog Number: M00421860TR0) 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
- M00421860TR0
- Product Code / EMDN
- OAD
- Device Name
- RF Cardiac Ablation Pod 100
- 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 Maestro 3000 RF Cardiac Ablation Pod 100?
The registered manufacturer of record for Maestro 3000 RF Cardiac Ablation Pod 100 is BOSTON SCIENTIFIC CORPORATION.
What is the Primary UDI-DI identifier for Maestro 3000 RF Cardiac Ablation Pod 100?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M00421860TR0.
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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