eudamed_udi
Primary ID: 04031815675226
NOBASHUCO® RUTSCHFEST (UDI 04031815675226)
Manufactured by NOBAMED Paul Danz AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NOBASHUCO® RUTSCHFEST - Primary ID 04031815675226
Device Regulatory Overview
The NOBASHUCO® RUTSCHFEST (Model/Catalog Number: 675101) is a medical device manufactured by NOBAMED Paul Danz AG. This product is indexed under FDA Product Code / Category Classification T0208 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 675101
- Product Code / EMDN
- T0208
- Device Name
- NOBASHUCO®
- Database Sync Date
- 2026-08-09 16:28:54
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 NOBASHUCO® RUTSCHFEST?
The registered manufacturer of record for NOBASHUCO® RUTSCHFEST is NOBAMED Paul Danz AG.
What is the Primary UDI-DI identifier for NOBASHUCO® RUTSCHFEST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031815675226.
What classification code is assigned to this device?
This device is registered under product classification code T0208.
Similar Classification Devices (T0208)
Other Devices by NOBAMED Paul Danz AG
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