gudid
Primary ID: 173
Liquichek (UDI 173)
Manufactured by BIO-RAD LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Liquichek - Primary ID 173
Device Regulatory Overview
The Liquichek (Model/Catalog Number: 173) is a medical device manufactured by BIO-RAD LABORATORIES, INC.. This product is indexed under FDA Product Code / Category Classification GGM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 173
- Product Code / EMDN
- GGM
- Device Name
- Liquichek Diabetes Control Level 3 (A human whole blood assayed diabetes control.)
- Database Sync Date
- 2026-08-09 09:48:17
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 Liquichek?
The registered manufacturer of record for Liquichek is BIO-RAD LABORATORIES, INC..
What is the Primary UDI-DI identifier for Liquichek?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 173.
What classification code is assigned to this device?
This device is registered under product classification code GGM.
Similar Classification Devices (GGM)
Other Devices by BIO-RAD LABORATORIES, INC.
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