GUDIDData
eudamed_udi Primary ID: 06972860120096

Refrigerated microcentrifuge (UDI 06972860120096)

Manufactured by RWD Life Science Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Refrigerated microcentrifuge - Primary ID 06972860120096

Device Regulatory Overview

The Refrigerated microcentrifuge (Model/Catalog Number: 91300) is a medical device manufactured by RWD Life Science Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W02069005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
91300
Product Code / EMDN
W02069005
Device Name
Microcentrifuge/Refrigerated microcentrifuge/High-Speed Benchtop Refrigerated Centrifuge
Database Sync Date
2026-08-09 16:28:53

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 Refrigerated microcentrifuge?

The registered manufacturer of record for Refrigerated microcentrifuge is RWD Life Science Co., Ltd..

What is the Primary UDI-DI identifier for Refrigerated microcentrifuge?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972860120096.

What classification code is assigned to this device?

This device is registered under product classification code W02069005.

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