KINCISE System Acetabular Cup Extraction Polymer Head 50mm (UDI KIN-2110-50-PP)
Manufactured by Spierings Orthopaedics B.V.
Device Regulatory Overview
The KINCISE System Acetabular Cup Extraction Polymer Head 50mm (Model/Catalog Number: KIN-2110-50-PP) is a medical device manufactured by Spierings Orthopaedics B.V.. This product is indexed under FDA Product Code / Category Classification HWE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KIN-2110-50-PP
- Product Code / EMDN
- HWE
- Device Name
- Database Sync Date
- 2026-08-09 09:26:43
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 KINCISE System Acetabular Cup Extraction Polymer Head 50mm?
The registered manufacturer of record for KINCISE System Acetabular Cup Extraction Polymer Head 50mm is Spierings Orthopaedics B.V..
What is the Primary UDI-DI identifier for KINCISE System Acetabular Cup Extraction Polymer Head 50mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KIN-2110-50-PP.
What classification code is assigned to this device?
This device is registered under product classification code HWE.
Similar Classification Devices (HWE)
Other Devices by Spierings Orthopaedics B.V.
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