HistoCore PELORIS (UDI HistoCore PELORIS 3 (100-120V))
Manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD
Device Regulatory Overview
The HistoCore PELORIS (Model/Catalog Number: HistoCore PELORIS 3 (100-120V)) 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 (100-120V)
- Product Code / EMDN
- IEO
- Device Name
- The HistoCore PELORIS 3 dual retort rapid tissue processor automates preparation of tissue samples for sectioning. This is achieved by transforming fixed specimens into wax infiltrated specimens by exposing them to a sequence of reagents in the tissue processor. Tissue samples subsequently undergo interpretation by a qualified healthcare professional to aid diagnosis.
- 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 (100-120V).
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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