gudid
Primary ID: DE408
Firefly (UDI DE408)
Manufactured by Firefly Global
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Firefly - Primary ID DE408
Device Regulatory Overview
The Firefly (Model/Catalog Number: DE408) is a medical device manufactured by Firefly Global. This product is indexed under FDA Product Code / Category Classification HRB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DE408
- Product Code / EMDN
- HRB
- Device Name
- Digital Iris Scope
- Database Sync Date
- 2026-08-09 09:49:36
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 Firefly?
The registered manufacturer of record for Firefly is Firefly Global.
What is the Primary UDI-DI identifier for Firefly?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DE408.
What classification code is assigned to this device?
This device is registered under product classification code HRB.
Similar Classification Devices (HRB)
Other Devices by Firefly Global
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