gudid
Primary ID: 45x75 N.1
Marienfeld Superior (UDI 45x75 N.1)
Manufactured by Paul Marienfeld GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Marienfeld Superior - Primary ID 45x75 N.1
Device Regulatory Overview
The Marienfeld Superior (Model/Catalog Number: 45x75 N.1) is a medical device manufactured by Paul Marienfeld GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification KES within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 45x75 N.1
- Product Code / EMDN
- KES
- 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 45x75 N.1.
What classification code is assigned to this device?
This device is registered under product classification code KES.
Similar Classification Devices (KES)
Other Devices by Paul Marienfeld GmbH & Co. KG
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