gudid
Primary ID: 26310MD
CLICKLINE (UDI 26310MD)
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 CLICKLINE - Primary ID 26310MD
Device Regulatory Overview
The CLICKLINE (Model/Catalog Number: 26310MD) is a medical device manufactured by Karl Storz GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification NWW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 26310MD
- Product Code / EMDN
- NWW
- Device Name
- CLICKLINE Forceps Insert
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CLICKLINE?
The registered manufacturer of record for CLICKLINE is Karl Storz GmbH & Co. KG.
What is the Primary UDI-DI identifier for CLICKLINE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26310MD.
What classification code is assigned to this device?
This device is registered under product classification code NWW.
Similar Classification Devices (NWW)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint