gudid
Primary ID: 823350
Lymphoscreen DR 30 x 2 (UDI 823350)
Manufactured by Bio-Rad Medical Diagnostics GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lymphoscreen DR 30 x 2 - Primary ID 823350
Device Regulatory Overview
The Lymphoscreen DR 30 x 2 (Model/Catalog Number: 823350) is a medical device manufactured by Bio-Rad Medical Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification MZI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 823350
- Product Code / EMDN
- MZI
- Device Name
- Human lymphocytes for 12 detections of human HLA-DR/DQ antibodies in the complement-dependent microlymphocytotoxicity test
- Database Sync Date
- 2026-08-09 09:48:49
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 Lymphoscreen DR 30 x 2?
The registered manufacturer of record for Lymphoscreen DR 30 x 2 is Bio-Rad Medical Diagnostics GmbH.
What is the Primary UDI-DI identifier for Lymphoscreen DR 30 x 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 823350.
What classification code is assigned to this device?
This device is registered under product classification code MZI.
Similar Classification Devices (MZI)
Other Devices by Bio-Rad Medical Diagnostics GmbH
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