Whole Blood Hemoglobin Determination (UDI KHG)
Device Regulatory Overview
The Whole Blood Hemoglobin Determination (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification KHG within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- KHG
- Device Name
- Whole Blood Hemoglobin Determination
- Database Sync Date
- 2026-08-09 09:00:27
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 Whole Blood Hemoglobin Determination?
The registered manufacturer of record for Whole Blood Hemoglobin Determination is .
What is the Primary UDI-DI identifier for Whole Blood Hemoglobin Determination?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KHG.
What classification code is assigned to this device?
This device is registered under product classification code KHG.
Programmatic Export
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JSON API Endpoint