GUDIDData
eudamed_udi Primary ID: 20845357022053

Unspecified Brand (UDI 20845357022053)

Manufactured by Microbiologics, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 20845357022053

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: [0897P] KWIK-STIK™ C. tropicalis ATCC 9968™) is a medical device manufactured by Microbiologics, INC.. This product is indexed under FDA Product Code / Category Classification W01040699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
[0897P] KWIK-STIK™ C. tropicalis ATCC 9968™
Product Code / EMDN
W01040699
Device Name
KWIK-STIK™ and LYFO DISK™
Database Sync Date
2026-08-09 16:30:41

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Microbiologics, INC..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20845357022053.

What classification code is assigned to this device?

This device is registered under product classification code W01040699.

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