GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: 303060-0146-000

I/A HANDPIECE, 21G CURVED (UDI 303060-0146-000)

Manufactured by Carl Zeiss Meditec AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for I/A HANDPIECE, 21G CURVED - Primary ID 303060-0146-000

Device Regulatory Overview

The I/A HANDPIECE, 21G CURVED (Model/Catalog Number: 303060-0146-000) is a medical device manufactured by Carl Zeiss Meditec AG. This product is indexed under FDA Product Code / Category Classification HQC 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-2649-2026 View Full Alert →

Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1153-2014 View Full Alert →

Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The VisuMax Laser K...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1049-2015 View Full Alert →

FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catalog numbers: 00000...

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

Technical Specifications

Model Number
303060-0146-000
Product Code / EMDN
HQC
Device Name
This single use device is an accessory for ZEISS phaco systems. It has been designed to remove the cortex and clean the capsule bag during human cataract surgery.
Database Sync Date
2026-08-09 09:11:22

Full Regulatory Attributes

🔒 Token Gated 
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of I/A HANDPIECE, 21G CURVED?

The registered manufacturer of record for I/A HANDPIECE, 21G CURVED is Carl Zeiss Meditec AG.

What is the Primary UDI-DI identifier for I/A HANDPIECE, 21G CURVED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 303060-0146-000.

What classification code is assigned to this device?

This device is registered under product classification code HQC.

Similar Classification Devices (HQC)

Other Devices by Carl Zeiss Meditec AG

Programmatic Export

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

JSON API Endpoint