gudid
Primary ID: 31500.0002
MAGNETOLITH (UDI 31500.0002)
Manufactured by Storz Medical AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MAGNETOLITH - Primary ID 31500.0002
Device Regulatory Overview
The MAGNETOLITH (Model/Catalog Number: 31500.0002) is a medical device manufactured by Storz Medical AG. This product is indexed under FDA Product Code / Category Classification IPF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 31500.0002
- Product Code / EMDN
- IPF
- Device Name
- Equipment for the extracorporeal magnetotransduction therapy.
- Database Sync Date
- 2026-08-09 09:03:25
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 MAGNETOLITH?
The registered manufacturer of record for MAGNETOLITH is Storz Medical AG.
What is the Primary UDI-DI identifier for MAGNETOLITH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 31500.0002.
What classification code is assigned to this device?
This device is registered under product classification code IPF.
Similar Classification Devices (IPF)
Other Devices by Storz Medical AG
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