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gudid Primary ID: 302721-9137-000

Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS (UDI 302721-9137-000)

Manufactured by Carl Zeiss Meditec AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS - Primary ID 302721-9137-000

Device Regulatory Overview

The Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS (Model/Catalog Number: 302721-9137-000) is a medical device manufactured by Carl Zeiss Meditec AG. This product is indexed under FDA Product Code / Category Classification HRM 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 →

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🔒 Compromised Lot & Serial Numbers Locked
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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
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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
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Technical Specifications

Model Number
302721-9137-000
Product Code / EMDN
HRM
Device Name
Single- use lenses for RESIGHT are ophthalmic surgical microscope lenses used in combination with the ZEISS RESIGHT fundus viewing system. The fundus viewing system is an accessory for surgical microscopes which is used for surgery on the posterior segment of the eye. It is used for stereoscopic imaging of the posterior segment and the retina.
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
}

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Frequently Asked Questions

Who is the primary manufacturer of Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS?

The registered manufacturer of record for Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS is Carl Zeiss Meditec AG.

What is the Primary UDI-DI identifier for Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 302721-9137-000.

What classification code is assigned to this device?

This device is registered under product classification code HRM.

Similar Classification Devices (HRM)

Other Devices by Carl Zeiss Meditec AG

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