gudid
Primary ID: 670266-KIT
Curaplex (UDI 670266-KIT)
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 670266-KIT
Device Regulatory Overview
The Curaplex (Model/Catalog Number: 670266-KIT) is a medical device manufactured by BOUND TREE MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification CBP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 670266-KIT
- Product Code / EMDN
- CBP
- Device Name
- ALLIED/CP ONLY Curaplex CPR AED Responder Kit, AED.com
- 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 670266-KIT.
What classification code is assigned to this device?
This device is registered under product classification code CBP.
Similar Classification Devices (CBP)
Other Devices by BOUND TREE MEDICAL, LLC
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