gudid
Primary ID: 110043025
Conflow Bone Cement (UDI 110043025)
Manufactured by TECRES SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Conflow Bone Cement - Primary ID 110043025
Device Regulatory Overview
The Conflow Bone Cement (Model/Catalog Number: 110043025) is a medical device manufactured by TECRES SPA. This product is indexed under FDA Product Code / Category Classification LOD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 110043025
- Product Code / EMDN
- LOD
- Device Name
- Conflow Bone Cement is a low viscosity polymethylmethacrylate bone cement. It is composed by two components (40g powder and 13,3g liquid) which are designed for mixing together at the point of use to form the cement. The device is supplied sterile, for single use. Conflow Bone Cement is indicated for the fixation of joint prosthesis implants to the host bone.
- Database Sync Date
- 2026-08-09 09:05:06
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 Conflow Bone Cement?
The registered manufacturer of record for Conflow Bone Cement is TECRES SPA.
What is the Primary UDI-DI identifier for Conflow Bone Cement?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 110043025.
What classification code is assigned to this device?
This device is registered under product classification code LOD.
Similar Classification Devices (LOD)
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