REFLECTO FEMORAL COMPONENT CEMENTED RIGHT SIZE 3 (UDI 05051659177020)
Manufactured by Covision Medical Technologies Ltd.
Device Regulatory Overview
The REFLECTO FEMORAL COMPONENT CEMENTED RIGHT SIZE 3 (Model/Catalog Number: 01.9726) is a medical device manufactured by Covision Medical Technologies Ltd.. This product is indexed under FDA Product Code / Category Classification P09090501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 01.9726
- Product Code / EMDN
- P09090501
- Device Name
- REFLECTO FEMORAL COMPONENT CEMENTED RIGHT SIZE 3
- Database Sync Date
- 2026-08-09 16:28:46
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 REFLECTO FEMORAL COMPONENT CEMENTED RIGHT SIZE 3?
The registered manufacturer of record for REFLECTO FEMORAL COMPONENT CEMENTED RIGHT SIZE 3 is Covision Medical Technologies Ltd..
What is the Primary UDI-DI identifier for REFLECTO FEMORAL COMPONENT CEMENTED RIGHT SIZE 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051659177020.
What classification code is assigned to this device?
This device is registered under product classification code P09090501.
Similar Classification Devices (P09090501)
Other Devices by Covision Medical Technologies Ltd.
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