gudid
Primary ID: 813170100
IH-Card Group ABO (UDI 813170100)
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 IH-Card Group ABO - Primary ID 813170100
Device Regulatory Overview
The IH-Card Group ABO (Model/Catalog Number: 813170100) is a medical device manufactured by Bio-Rad Medical Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 813170100
- Product Code / EMDN
- N/A
- Device Name
- Gel card for use with the IH-system; Card for ABO antigen typing; 12 cards of 6 microtubes
- 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 IH-Card Group ABO?
The registered manufacturer of record for IH-Card Group ABO is Bio-Rad Medical Diagnostics GmbH.
What is the Primary UDI-DI identifier for IH-Card Group ABO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 813170100.
What classification code is assigned to this device?
This device is registered under product classification code .
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