eudamed_udi
Primary ID: 09343044006579
RIDA®Plex Viral 8 well Step 2 (UDI 09343044006579)
Manufactured by AusDiagnostics Pty Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RIDA®Plex Viral 8 well Step 2 - Primary ID 09343044006579
Device Regulatory Overview
The RIDA®Plex Viral 8 well Step 2 (Model/Catalog Number: 27093P) is a medical device manufactured by AusDiagnostics Pty Ltd. This product is indexed under FDA Product Code / Category Classification W0105070399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 27093P
- Product Code / EMDN
- W0105070399
- Device Name
- RIDA®Plex Viral 8 well
- Database Sync Date
- 2026-08-09 17:44:29
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 Viral 8 well Step 2?
The registered manufacturer of record for RIDA®Plex Viral 8 well Step 2 is AusDiagnostics Pty Ltd.
What is the Primary UDI-DI identifier for RIDA®Plex Viral 8 well Step 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09343044006579.
What classification code is assigned to this device?
This device is registered under product classification code W0105070399.
Similar Classification Devices (W0105070399)
Other Devices by AusDiagnostics Pty Ltd
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