GUDIDData
eudamed_udi Primary ID: 06976117454545

Fibrin and Fibrinogen Degradation Products Calibrator (UDI 06976117454545)

Manufactured by Shenzhen Dymind Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fibrin and Fibrinogen Degradation Products Calibrator - Primary ID 06976117454545

Device Regulatory Overview

The Fibrin and Fibrinogen Degradation Products Calibrator (Model/Catalog Number: NX-0014-04) is a medical device manufactured by Shenzhen Dymind Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0103020701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NX-0014-04
Product Code / EMDN
W0103020701
Device Name
Fibrin and Fibrinogen Degradation Products Calibrator
Database Sync Date
2026-08-09 16:29:50

Full Regulatory Attributes

πŸ”’ 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 Fibrin and Fibrinogen Degradation Products Calibrator?

The registered manufacturer of record for Fibrin and Fibrinogen Degradation Products Calibrator is Shenzhen Dymind Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for Fibrin and Fibrinogen Degradation Products Calibrator?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976117454545.

What classification code is assigned to this device?

This device is registered under product classification code W0103020701.

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