GUDIDData
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emdn_classification Primary ID: Q0210030103

READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES (UDI Q0210030103)

Manufactured by

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES - Primary ID Q0210030103

Device Regulatory Overview

The READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification Q0210030103 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-2753-2026 View Full Alert →

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Technical Specifications

Model Number
N/A
Product Code / EMDN
Q0210030103
Device Name
READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES
Database Sync Date
2026-08-09 16:18:37

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 READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES?

The registered manufacturer of record for READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES is .

What is the Primary UDI-DI identifier for READY TO WEAR METAL AND PLASTIC SPECTACLES WITH ORGANIC LENSES?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Q0210030103.

What classification code is assigned to this device?

This device is registered under product classification code Q0210030103.

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