gudid
Primary ID: 69642
Flents (UDI 69642)
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 69642
Device Regulatory Overview
The Flents (Model/Catalog Number: 69642) is a medical device manufactured by APOTHECARY PRODUCTS, LLC. This product is indexed under FDA Product Code / Category Classification CAE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 69642
- Product Code / EMDN
- CAE
- Device Name
- CPR MICROSHIELD 2/24
- 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 69642.
What classification code is assigned to this device?
This device is registered under product classification code CAE.
Similar Classification Devices (CAE)
Other Devices by APOTHECARY PRODUCTS, LLC
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