gudid
Primary ID: 13927NKS
SILVER SCOPE (UDI 13927NKS)
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 SILVER SCOPE - Primary ID 13927NKS
Device Regulatory Overview
The SILVER SCOPE (Model/Catalog Number: 13927NKS) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification FDF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13927NKS
- Product Code / EMDN
- FDF
- Device Name
- Slim colonoscpe 11,2/3,4/1530 NTSC
- Database Sync Date
- 2026-08-09 09:11:32
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 SILVER SCOPE?
The registered manufacturer of record for SILVER SCOPE is Karl Storz GmbH & Co. KG.
What is the Primary UDI-DI identifier for SILVER SCOPE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13927NKS.
What classification code is assigned to this device?
This device is registered under product classification code FDF.
Similar Classification Devices (FDF)
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