gudid
Primary ID: 740
Lyphochek (UDI 740)
Manufactured by BIO-RAD LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lyphochek - Primary ID 740
Device Regulatory Overview
The Lyphochek (Model/Catalog Number: 740) 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
- 740
- Product Code / EMDN
- GGM
- Device Name
- Lyphochek Diabetes Control Bilevel (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 Lyphochek?
The registered manufacturer of record for Lyphochek is BIO-RAD LABORATORIES, INC..
What is the Primary UDI-DI identifier for Lyphochek?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 740.
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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