gudid Primary ID: KIN-2110-54-PP

KINCISE System Acetabular Cup Extraction Polymer Head 54mm (UDI KIN-2110-54-PP)

Manufactured by Spierings Orthopaedics B.V.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The KINCISE System Acetabular Cup Extraction Polymer Head 54mm (Model/Catalog Number: KIN-2110-54-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-2110-54-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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Frequently Asked Questions

Who is the primary manufacturer of KINCISE System Acetabular Cup Extraction Polymer Head 54mm?

The registered manufacturer of record for KINCISE System Acetabular Cup Extraction Polymer Head 54mm is Spierings Orthopaedics B.V..

What is the Primary UDI-DI identifier for KINCISE System Acetabular Cup Extraction Polymer Head 54mm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KIN-2110-54-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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