gudid
Primary ID: TH201
NA (UDI TH201)
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 TH201
Device Regulatory Overview
The NA (Model/Catalog Number: TH201) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification OWN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TH201
- Product Code / EMDN
- OWN
- Device Name
- VITOM EAGLE
- Database Sync Date
- 2026-08-09 09:11:31
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 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 TH201.
What classification code is assigned to this device?
This device is registered under product classification code OWN.
Similar Classification Devices (OWN)
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