Single Use Electrosurgical Hemostatic Forceps (UDI FD-412LR)
Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.
Device Regulatory Overview
The Single Use Electrosurgical Hemostatic Forceps (Model/Catalog Number: FD-412LR) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FD-412LR
- Product Code / EMDN
- KGE
- Device Name
- Database Sync Date
- 2026-08-09 09:46:01
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 Single Use Electrosurgical Hemostatic Forceps?
The registered manufacturer of record for Single Use Electrosurgical Hemostatic Forceps is OLYMPUS MEDICAL SYSTEMS CORP..
What is the Primary UDI-DI identifier for Single Use Electrosurgical Hemostatic Forceps?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FD-412LR.
What classification code is assigned to this device?
This device is registered under product classification code KGE.
Similar Classification Devices (KGE)
Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.
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