gudid
Primary ID: 1015-47153
Curaplex (UDI 1015-47153)
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 1015-47153
Device Regulatory Overview
The Curaplex (Model/Catalog Number: 1015-47153) is a medical device manufactured by BOUND TREE MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification QDO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1015-47153
- Product Code / EMDN
- QDO
- Device Name
- TritonGrip HV Gloves, Exam, Nitrile, Non-Sterile, Powder-Free, Textured, Orange, L
- 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 1015-47153.
What classification code is assigned to this device?
This device is registered under product classification code QDO.
Similar Classification Devices (QDO)
Other Devices by BOUND TREE MEDICAL, LLC
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