GUDIDData
gudid Primary ID: ZIC-CMBO-2RT3

Zip-IQ Combo digital centrifuge with hematocrit and test tube rotors (UDI ZIC-CMBO-2RT3)

Manufactured by LW SCIENTIFIC, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zip-IQ Combo digital centrifuge with hematocrit and test tube rotors - Primary ID ZIC-CMBO-2RT3

Device Regulatory Overview

The Zip-IQ Combo digital centrifuge with hematocrit and test tube rotors (Model/Catalog Number: ZIC-CMBO-2RT3) is a medical device manufactured by LW SCIENTIFIC, INC.. This product is indexed under FDA Product Code / Category Classification GKG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ZIC-CMBO-2RT3
Product Code / EMDN
GKG
Device Name
Zip-IQ Combo Centrifuge, digital, 2 rotors, 6pl angled TT (15ml) and 24pl crit (75mm) rotors, 90-240v
Database Sync Date
2026-08-09 09:17:27

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 Zip-IQ Combo digital centrifuge with hematocrit and test tube rotors?

The registered manufacturer of record for Zip-IQ Combo digital centrifuge with hematocrit and test tube rotors is LW SCIENTIFIC, INC..

What is the Primary UDI-DI identifier for Zip-IQ Combo digital centrifuge with hematocrit and test tube rotors?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZIC-CMBO-2RT3.

What classification code is assigned to this device?

This device is registered under product classification code GKG.

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