gudid
Primary ID: W003
Ragweed, Giant Ambrosia trifida (UDI W003)
Manufactured by HYCOR BIOMEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ragweed, Giant Ambrosia trifida - Primary ID W003
Device Regulatory Overview
The Ragweed, Giant Ambrosia trifida (Model/Catalog Number: W003) 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
- W003
- 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 Ragweed, Giant Ambrosia trifida?
The registered manufacturer of record for Ragweed, Giant Ambrosia trifida is HYCOR BIOMEDICAL LLC.
What is the Primary UDI-DI identifier for Ragweed, Giant Ambrosia trifida?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W003.
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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