gudid
Primary ID: 71207
SPECIFIC IGE CONTROL KIT (UDI 71207)
Manufactured by HYCOR BIOMEDICAL LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SPECIFIC IGE CONTROL KIT - Primary ID 71207
Device Regulatory Overview
The SPECIFIC IGE CONTROL KIT (Model/Catalog Number: 71207) 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
- 71207
- Product Code / EMDN
- DGC
- Device Name
- 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 SPECIFIC IGE CONTROL KIT?
The registered manufacturer of record for SPECIFIC IGE CONTROL KIT is HYCOR BIOMEDICAL LLC.
What is the Primary UDI-DI identifier for SPECIFIC IGE CONTROL KIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 71207.
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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