gudid
Primary ID: F405-620
FLENTS (UDI F405-620)
Manufactured by APOTHECARY PRODUCTS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLENTS - Primary ID F405-620
Device Regulatory Overview
The FLENTS (Model/Catalog Number: F405-620) is a medical device manufactured by APOTHECARY PRODUCTS, LLC. This product is indexed under FDA Product Code / Category Classification FXX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F405-620
- Product Code / EMDN
- FXX
- Device Name
- 620 EARLOOP MASK
- Database Sync Date
- 2026-08-09 09:00:33
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 FLENTS?
The registered manufacturer of record for FLENTS is APOTHECARY PRODUCTS, LLC.
What is the Primary UDI-DI identifier for FLENTS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is F405-620.
What classification code is assigned to this device?
This device is registered under product classification code FXX.
Similar Classification Devices (FXX)
Other Devices by APOTHECARY PRODUCTS, LLC
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