gudid
Primary ID: 24941A
TEO (UDI 24941A)
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 TEO - Primary ID 24941A
Device Regulatory Overview
The TEO (Model/Catalog Number: 24941A) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification GCF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 24941A
- Product Code / EMDN
- GCF
- Device Name
- TEO Working Attachment for 24941 T
- Database Sync Date
- 2026-08-09 10:02:14
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 TEO?
The registered manufacturer of record for TEO is Karl Storz GmbH & Co. KG.
What is the Primary UDI-DI identifier for TEO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 24941A.
What classification code is assigned to this device?
This device is registered under product classification code GCF.
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