GUDIDData
gudid Primary ID: AD750SC-KE40

Advincula Delineator Uterine Manipulator (UDI AD750SC-KE40)

Manufactured by Coopersurgical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Advincula Delineator Uterine Manipulator - Primary ID AD750SC-KE40

Device Regulatory Overview

The Advincula Delineator Uterine Manipulator (Model/Catalog Number: AD750SC-KE40) is a medical device manufactured by Coopersurgical, Inc.. This product is indexed under FDA Product Code / Category Classification HEW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AD750SC-KE40
Product Code / EMDN
HEW
Device Name
Advincula Delineator Uterine Manipulator with 4.0cm Soft Koh-Efficient
Database Sync Date
2026-08-09 09:19:29

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Advincula Delineator Uterine Manipulator?

The registered manufacturer of record for Advincula Delineator Uterine Manipulator is Coopersurgical, Inc..

What is the Primary UDI-DI identifier for Advincula Delineator Uterine Manipulator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AD750SC-KE40.

What classification code is assigned to this device?

This device is registered under product classification code HEW.

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