GUDIDData
eudamed_udi Primary ID: 06942826214381

CITOGLAS (UDI 06942826214381)

Manufactured by CITOTEST LABWARE MANUFACTURING CO.,LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CITOGLAS - Primary ID 06942826214381

Device Regulatory Overview

The CITOGLAS (Model/Catalog Number: 0345-1420) is a medical device manufactured by CITOTEST LABWARE MANUFACTURING CO.,LTD. This product is indexed under FDA Product Code / Category Classification W0503900202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0345-1420
Product Code / EMDN
W0503900202
Device Name
Microscope Cover Glass
Database Sync Date
2026-08-09 16:29:37

Full Regulatory Attributes

πŸ”’ 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 CITOGLAS?

The registered manufacturer of record for CITOGLAS is CITOTEST LABWARE MANUFACTURING CO.,LTD.

What is the Primary UDI-DI identifier for CITOGLAS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942826214381.

What classification code is assigned to this device?

This device is registered under product classification code W0503900202.

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