gudid
Primary ID: W008
Dandelion Taraxacum officinale (UDI W008)
Manufactured by HYCOR BIOMEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dandelion Taraxacum officinale - Primary ID W008
Device Regulatory Overview
The Dandelion Taraxacum officinale (Model/Catalog Number: W008) is a medical device manufactured by HYCOR BIOMEDICAL LLC. This product is indexed under FDA Product Code / Category Classification DGC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W008
- Product Code / EMDN
- DGC
- Device Name
- A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of an allergen specific immunoglobulin E (IgE) antibody in a clinical specimen.
- Database Sync Date
- 2026-08-09 09:31:26
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 Dandelion Taraxacum officinale?
The registered manufacturer of record for Dandelion Taraxacum officinale is HYCOR BIOMEDICAL LLC.
What is the Primary UDI-DI identifier for Dandelion Taraxacum officinale?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W008.
What classification code is assigned to this device?
This device is registered under product classification code DGC.
Similar Classification Devices (DGC)
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