GUDIDData
eudamed_udi Primary ID: 08683555618634

CALCIUM Kit (UDI 08683555618634)

Manufactured by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CALCIUM Kit - Primary ID 08683555618634

Device Regulatory Overview

The CALCIUM Kit (Model/Catalog Number: B28066) is a medical device manufactured by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification W01010303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
B28066
Product Code / EMDN
W01010303
Device Name
CALCIUM Kit
Database Sync Date
2026-08-09 17:38:52

Full Regulatory Attributes

🔒 Token Gated
{
    "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 CALCIUM Kit?

The registered manufacturer of record for CALCIUM Kit is KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for CALCIUM Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683555618634.

What classification code is assigned to this device?

This device is registered under product classification code W01010303.

Similar Classification Devices (W01010303)

Other Devices by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ

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