gudid
Primary ID: 10973HD
NA (UDI 10973HD)
Manufactured by Karl Storz GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID 10973HD
Device Regulatory Overview
The NA (Model/Catalog Number: 10973HD) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification EWY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10973HD
- Product Code / EMDN
- EWY
- Device Name
- Video Mediastinoscope
- Database Sync Date
- 2026-08-09 09:11:31
Full Regulatory Attributes
🔒 Token Gated
{
"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 NA?
The registered manufacturer of record for NA is Karl Storz GmbH & Co. KG.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10973HD.
What classification code is assigned to this device?
This device is registered under product classification code EWY.
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