HistoCore PELORIS (UDI HistoCore PELORIS 3 Win10 Upgrade Kit)
Manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD
Device Regulatory Overview
The HistoCore PELORIS (Model/Catalog Number: HistoCore PELORIS 3 Win10 Upgrade Kit) is a medical device manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD. This product is indexed under FDA Product Code / Category Classification IEO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HistoCore PELORIS 3 Win10 Upgrade Kit
- Product Code / EMDN
- IEO
- Device Name
- HistoCore PELORIS 3 Win10 Upgrade Kit
- Database Sync Date
- 2026-08-09 09:38:27
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of HistoCore PELORIS?
The registered manufacturer of record for HistoCore PELORIS is LEICA BIOSYSTEMS MELBOURNE PTY LTD.
What is the Primary UDI-DI identifier for HistoCore PELORIS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HistoCore PELORIS 3 Win10 Upgrade Kit.
What classification code is assigned to this device?
This device is registered under product classification code IEO.
Similar Classification Devices (IEO)
Other Devices by LEICA BIOSYSTEMS MELBOURNE PTY LTD
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