Single Use 3-Lumen Sphincterotome V (UDI KD-V431M-0720)
Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.
Device Regulatory Overview
The Single Use 3-Lumen Sphincterotome V (Model/Catalog Number: KD-V431M-0720) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification KNS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KD-V431M-0720
- Product Code / EMDN
- KNS
- Device Name
- Single Use 3-Lumen Sphincterotome V
- 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 3-Lumen Sphincterotome V?
The registered manufacturer of record for Single Use 3-Lumen Sphincterotome V is OLYMPUS MEDICAL SYSTEMS CORP..
What is the Primary UDI-DI identifier for Single Use 3-Lumen Sphincterotome V?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KD-V431M-0720.
What classification code is assigned to this device?
This device is registered under product classification code KNS.
Similar Classification Devices (KNS)
Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.
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