GUDIDData
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eudamed_udi Primary ID: 00814247020017

ClearView Uterine Manipulator 7cm tip (UDI 00814247020017)

Manufactured by Clinical Innovations, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearView Uterine Manipulator 7cm tip - Primary ID 00814247020017

Device Regulatory Overview

The ClearView Uterine Manipulator 7cm tip (Model/Catalog Number: UM700) is a medical device manufactured by Clinical Innovations, LLC. This product is indexed under FDA Product Code / Category Classification Z120899 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1945-2026 View Full Alert →

Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number: VAC-6000MT Product Descrip...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-0541-2021 View Full Alert →

Clinical Innovations ROM Plus Collection Kit IFU: ROM Plus Rupture of Membrane Test ROM-5025, ROM-6025...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-0123-2016 View Full Alert →

The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or reduction of postpartu...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
UM700
Product Code / EMDN
Z120899
Device Name
ClearView Uterine Manipulator
Database Sync Date
2026-08-09 17:03:29

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 ClearView Uterine Manipulator 7cm tip?

The registered manufacturer of record for ClearView Uterine Manipulator 7cm tip is Clinical Innovations, LLC.

What is the Primary UDI-DI identifier for ClearView Uterine Manipulator 7cm tip?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00814247020017.

What classification code is assigned to this device?

This device is registered under product classification code Z120899.

Similar Classification Devices (Z120899)

Other Devices by Clinical Innovations, LLC

Programmatic Export

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