gudid
Primary ID: UI500
ENDOFLATOR (UDI UI500)
Manufactured by Karl Storz GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ENDOFLATOR - Primary ID UI500
Device Regulatory Overview
The ENDOFLATOR (Model/Catalog Number: UI500) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification FCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UI500
- Product Code / EMDN
- FCX
- Device Name
- ENDOFLATOR 50
- Database Sync Date
- 2026-08-09 09:11:33
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 ENDOFLATOR?
The registered manufacturer of record for ENDOFLATOR is Karl Storz GmbH & Co. KG.
What is the Primary UDI-DI identifier for ENDOFLATOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UI500.
What classification code is assigned to this device?
This device is registered under product classification code FCX.
Similar Classification Devices (FCX)
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