gudid
Primary ID: OneScope Pro
Curaplex (UDI OneScope Pro)
Manufactured by BOUND TREE MEDICAL, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Curaplex - Primary ID OneScope Pro
Device Regulatory Overview
The Curaplex (Model/Catalog Number: OneScope Pro) is a medical device manufactured by BOUND TREE MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification LRC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OneScope Pro
- Product Code / EMDN
- LRC
- Device Name
- OneScope Pro Video Laryngoscope
- Database Sync Date
- 2026-08-09 09:09:51
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 Curaplex?
The registered manufacturer of record for Curaplex is BOUND TREE MEDICAL, LLC.
What is the Primary UDI-DI identifier for Curaplex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is OneScope Pro.
What classification code is assigned to this device?
This device is registered under product classification code LRC.
Similar Classification Devices (LRC)
Other Devices by BOUND TREE MEDICAL, LLC
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