gudid
Primary ID: 24912O
RECTOVISION (UDI 24912O)
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 RECTOVISION - Primary ID 24912O
Device Regulatory Overview
The RECTOVISION (Model/Catalog Number: 24912O) 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
- 24912O
- Product Code / EMDN
- GCF
- Device Name
- Obturator, for 24912
- 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 RECTOVISION?
The registered manufacturer of record for RECTOVISION is Karl Storz GmbH & Co. KG.
What is the Primary UDI-DI identifier for RECTOVISION?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 24912O.
What classification code is assigned to this device?
This device is registered under product classification code GCF.
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