eudamed_udi Primary ID: 08032986351250

VeressC (UDI 08032986351250)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VeressC (Model/Catalog Number: AVC1410) is a medical device manufactured by M.D.L. S.r.l.. This product is indexed under FDA Product Code / Category Classification K0104 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-2493-2021 View Full Alert →

General Manual surgical instrument...

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ID: Z-2492-2021 View Full Alert →

Soft Tissue Biopsy Needles...

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ID: Z-2491-2021 View Full Alert →

Mammary Nodules Localization...

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Technical Specifications

Model Number: AVC1410
Product Code / EMDN: K0104
Device Name: VeressC
Database Sync Date: 2026-08-09 18:25:40

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 VeressC?

The registered manufacturer of record for VeressC is M.D.L. S.r.l..

What is the Primary UDI-DI identifier for VeressC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08032986351250.

What classification code is assigned to this device?

This device is registered under product classification code K0104.

Similar Classification Devices (K0104)

Other Devices by M.D.L. S.r.l.

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