eudamed_udi
Primary ID: 04048551047705
Unspecified Brand (UDI 04048551047705)
Manufactured by KARL STORZ SE & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04048551047705
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 10379KF) is a medical device manufactured by KARL STORZ SE & Co. KG. This product is indexed under FDA Product Code / Category Classification L03130401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10379KF
- Product Code / EMDN
- L03130401
- Device Name
- Rigid/optical grasping forceps, bronchoscopy
- Database Sync Date
- 2026-08-09 16:29:11
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is KARL STORZ SE & Co. KG.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04048551047705.
What classification code is assigned to this device?
This device is registered under product classification code L03130401.
Similar Classification Devices (L03130401)
Other Devices by KARL STORZ SE & Co. KG
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint