Fujifilm Diathermic Slitter (FlushKnife) (UDI DK2623J -N20-)
Manufactured by FUJIFILM CORPORATION
Device Regulatory Overview
The Fujifilm Diathermic Slitter (FlushKnife) (Model/Catalog Number: DK2623J -N20-) is a medical device manufactured by FUJIFILM CORPORATION. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DK2623J -N20-
- Product Code / EMDN
- KGE
- Device Name
- These instruments have been designed to be used with specified endoscopes to cut tissue using high-frequency current within the digestive tract. Both the ball tip type and the needle type instruments are indicated for ablation, incision, dissection, avulsion, cauterization, coagulation and hemostasis of tissue within the digestive tract.
- Database Sync Date
- 2026-08-09 09:53:07
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 Fujifilm Diathermic Slitter (FlushKnife)?
The registered manufacturer of record for Fujifilm Diathermic Slitter (FlushKnife) is FUJIFILM CORPORATION.
What is the Primary UDI-DI identifier for Fujifilm Diathermic Slitter (FlushKnife)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DK2623J -N20-.
What classification code is assigned to this device?
This device is registered under product classification code KGE.
Similar Classification Devices (KGE)
Other Devices by FUJIFILM CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint