GUDIDData
eudamed_udi Primary ID: 05905386360517

Refrigerated and heated laboratory centrifuge MPW-352RH 100V/60Hz (UDI 05905386360517)

Manufactured by "MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Refrigerated and heated laboratory centrifuge MPW-352RH 100V/60Hz - Primary ID 05905386360517

Device Regulatory Overview

The Refrigerated and heated laboratory centrifuge MPW-352RH 100V/60Hz (Model/Catalog Number: 10352RH/1-6/100) is a medical device manufactured by "MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY. This product is indexed under FDA Product Code / Category Classification W02069005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10352RH/1-6/100
Product Code / EMDN
W02069005
Device Name
Refrigerated and heated laboratory centrifuge MPW-352RH
Database Sync Date
2026-08-09 16:48:35

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 and heated laboratory centrifuge MPW-352RH 100V/60Hz?

The registered manufacturer of record for Refrigerated and heated laboratory centrifuge MPW-352RH 100V/60Hz is "MPW MED. INSTRUMENTS" SPÓŁDZIELNIA PRACY.

What is the Primary UDI-DI identifier for Refrigerated and heated laboratory centrifuge MPW-352RH 100V/60Hz?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05905386360517.

What classification code is assigned to this device?

This device is registered under product classification code W02069005.

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