Marienfeld Superior (UDI HistoBond ground edges clipped corners)
Manufactured by Paul Marienfeld GmbH & Co. KG
Device Regulatory Overview
The Marienfeld Superior (Model/Catalog Number: HistoBond ground edges clipped corners) is a medical device manufactured by Paul Marienfeld GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification KEW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HistoBond ground edges clipped corners
- Product Code / EMDN
- KEW
- Device Name
- Database Sync Date
- 2026-08-09 09:11:40
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 Marienfeld Superior?
The registered manufacturer of record for Marienfeld Superior is Paul Marienfeld GmbH & Co. KG.
What is the Primary UDI-DI identifier for Marienfeld Superior?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HistoBond ground edges clipped corners.
What classification code is assigned to this device?
This device is registered under product classification code KEW.
Similar Classification Devices (KEW)
Other Devices by Paul Marienfeld GmbH & Co. KG
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