RIDA®Plex Parasites 8 well Step 2 (UDI 09343044006357)
Manufactured by AusDiagnostics Pty Ltd
Device Regulatory Overview
The RIDA®Plex Parasites 8 well Step 2 (Model/Catalog Number: 85021P) is a medical device manufactured by AusDiagnostics Pty Ltd. This product is indexed under FDA Product Code / Category Classification W01050704 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 85021P
- Product Code / EMDN
- W01050704
- Device Name
- RIDA®Plex Parasites 8 well
- Database Sync Date
- 2026-08-09 17:01:59
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 RIDA®Plex Parasites 8 well Step 2?
The registered manufacturer of record for RIDA®Plex Parasites 8 well Step 2 is AusDiagnostics Pty Ltd.
What is the Primary UDI-DI identifier for RIDA®Plex Parasites 8 well Step 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09343044006357.
What classification code is assigned to this device?
This device is registered under product classification code W01050704.
Similar Classification Devices (W01050704)
Other Devices by AusDiagnostics Pty Ltd
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