eudamed_udi
Primary ID: +G1202S017380N
Apex (UDI +G1202S017380N)
Manufactured by Falcon Surgical Co. (Pvt.) Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Apex - Primary ID +G1202S017380N
Device Regulatory Overview
The Apex (Model/Catalog Number: 2S01738) is a medical device manufactured by Falcon Surgical Co. (Pvt.) Ltd. This product is indexed under FDA Product Code / Category Classification L159009 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2S01738
- Product Code / EMDN
- L159009
- Device Name
- DENTAL FILES
- Database Sync Date
- 2026-08-09 16:29:01
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 Apex?
The registered manufacturer of record for Apex is Falcon Surgical Co. (Pvt.) Ltd.
What is the Primary UDI-DI identifier for Apex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G1202S017380N.
What classification code is assigned to this device?
This device is registered under product classification code L159009.
Similar Classification Devices (L159009)
Other Devices by Falcon Surgical Co. (Pvt.) Ltd
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