eudamed_udi Primary ID: 00630238008877

OLV-9 Woldoff Prismatic Biconcave Vitrectomy Lens (UDI 00630238008877)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The OLV-9 Woldoff Prismatic Biconcave Vitrectomy Lens (Model/Catalog Number: 887) is a medical device manufactured by Ocular Instruments Inc.. This product is indexed under FDA Product Code / Category Classification Q0299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 887
Product Code / EMDN: Q0299
Device Name: Contact Ophthalmic
Database Sync Date: 2026-08-09 16:29:04

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 OLV-9 Woldoff Prismatic Biconcave Vitrectomy Lens?

The registered manufacturer of record for OLV-9 Woldoff Prismatic Biconcave Vitrectomy Lens is Ocular Instruments Inc..

What is the Primary UDI-DI identifier for OLV-9 Woldoff Prismatic Biconcave Vitrectomy Lens?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00630238008877.

What classification code is assigned to this device?

This device is registered under product classification code Q0299.

Similar Classification Devices (Q0299)

Other Devices by Ocular Instruments Inc.

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