gudid Primary ID: KD-VC631Q-07203A

Single Use Preloaded Sphincterotome V(Distal Wireguided) (UDI KD-VC631Q-07203A)

Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Single Use Preloaded Sphincterotome V(Distal Wireguided) (Model/Catalog Number: KD-VC631Q-07203A) 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-VC631Q-07203A
Product Code / EMDN: KNS
Device Name: Single Use Preloaded Sphincterotome V(Distal Wireguided)
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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Frequently Asked Questions

Who is the primary manufacturer of Single Use Preloaded Sphincterotome V(Distal Wireguided)?

The registered manufacturer of record for Single Use Preloaded Sphincterotome V(Distal Wireguided) is OLYMPUS MEDICAL SYSTEMS CORP..

What is the Primary UDI-DI identifier for Single Use Preloaded Sphincterotome V(Distal Wireguided)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KD-VC631Q-07203A.

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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