GUDIDData
eudamed_udi Primary ID: 06924030402754

BioCLIA Autoimmune Reagent Kit, CENP-B (UDI 06924030402754)

Manufactured by HOB Biotech Group Corp., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioCLIA Autoimmune Reagent Kit, CENP-B - Primary ID 06924030402754

Device Regulatory Overview

The BioCLIA Autoimmune Reagent Kit, CENP-B (Model/Catalog Number: MY00160) is a medical device manufactured by HOB Biotech Group Corp., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102100199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MY00160
Product Code / EMDN
W0102100199
Device Name
BioCLIA Autoimmune Reagent Kit, CENP-B
Database Sync Date
2026-08-09 16:29:05

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of BioCLIA Autoimmune Reagent Kit, CENP-B?

The registered manufacturer of record for BioCLIA Autoimmune Reagent Kit, CENP-B is HOB Biotech Group Corp., Ltd..

What is the Primary UDI-DI identifier for BioCLIA Autoimmune Reagent Kit, CENP-B?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06924030402754.

What classification code is assigned to this device?

This device is registered under product classification code W0102100199.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint