gudid
Primary ID: M490006
SmartAblateTM System (UDI M490006)
Manufactured by Stockert GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SmartAblateTM System - Primary ID M490006
Device Regulatory Overview
The SmartAblateTM System (Model/Catalog Number: M490006) is a medical device manufactured by Stockert GmbH. This product is indexed under FDA Product Code / Category Classification LPB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M490006
- Product Code / EMDN
- LPB
- Device Name
- Database Sync Date
- 2026-08-09 09:17:35
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 SmartAblateTM System?
The registered manufacturer of record for SmartAblateTM System is Stockert GmbH.
What is the Primary UDI-DI identifier for SmartAblateTM System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M490006.
What classification code is assigned to this device?
This device is registered under product classification code LPB.
Similar Classification Devices (LPB)
Other Devices by Stockert GmbH
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