gudid
Primary ID: DE608
Firefly (UDI DE608)
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 DE608
Device Regulatory Overview
The Firefly (Model/Catalog Number: DE608) is a medical device manufactured by Firefly Global. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DE608
- Product Code / EMDN
- KYT
- Device Name
- General Exam Camera
- 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 DE608.
What classification code is assigned to this device?
This device is registered under product classification code KYT.
Similar Classification Devices (KYT)
Other Devices by Firefly Global
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