GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 08032986352004

CytoCut (UDI 08032986352004)

Manufactured by M.D.L. S.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CytoCut - Primary ID 08032986352004

Device Regulatory Overview

The CytoCut (Model/Catalog Number: PB2012) is a medical device manufactured by M.D.L. S.r.l.. This product is indexed under FDA Product Code / Category Classification A01020102 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...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2492-2021 View Full Alert →

Soft Tissue Biopsy Needles...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2491-2021 View Full Alert →

Mammary Nodules Localization...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
PB2012
Product Code / EMDN
A01020102
Device Name
CytoCut
Database Sync Date
2026-08-09 16:28:48

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 CytoCut?

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

What is the Primary UDI-DI identifier for CytoCut?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08032986352004.

What classification code is assigned to this device?

This device is registered under product classification code A01020102.

Similar Classification Devices (A01020102)

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint