eudamed_udi
Primary ID: 04251790238173
NC Osier™ (UDI 04251790238173)
Manufactured by SWL Medizin GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NC Osier™ - Primary ID 04251790238173
Device Regulatory Overview
The NC Osier™ (Model/Catalog Number: CDC843817) is a medical device manufactured by SWL Medizin GmbH. This product is indexed under FDA Product Code / Category Classification C010401020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CDC843817
- Product Code / EMDN
- C010401020101
- Device Name
- Balloon Dilatation Catheter
- Database Sync Date
- 2026-08-09 16:28:44
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 NC Osier™?
The registered manufacturer of record for NC Osier™ is SWL Medizin GmbH.
What is the Primary UDI-DI identifier for NC Osier™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251790238173.
What classification code is assigned to this device?
This device is registered under product classification code C010401020101.
Similar Classification Devices (C010401020101)
Other Devices by SWL Medizin GmbH
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