gudid
Primary ID: 824035
Hanks Solution (UDI 824035)
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 Hanks Solution - Primary ID 824035
Device Regulatory Overview
The Hanks Solution (Model/Catalog Number: 824035) is a medical device manufactured by Bio-Rad Medical Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification KIT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 824035
- Product Code / EMDN
- KIT
- Device Name
- For washing of lymphocytes in the microlymphocytotoxicity test, free of Ca and Mg, not for infusion
- 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 Hanks Solution?
The registered manufacturer of record for Hanks Solution is Bio-Rad Medical Diagnostics GmbH.
What is the Primary UDI-DI identifier for Hanks Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 824035.
What classification code is assigned to this device?
This device is registered under product classification code KIT.
Similar Classification Devices (KIT)
Other Devices by Bio-Rad Medical Diagnostics GmbH
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