GUDIDData
eudamed_udi Primary ID: D-KR-B2-MG-01100CAV

INNODX ß2-MG CMIA (UDI D-KR-B2-MG-01100CAV)

Manufactured by Xiamen Innodx Biotech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INNODX ß2-MG CMIA - Primary ID D-KR-B2-MG-01100CAV

Device Regulatory Overview

The INNODX ß2-MG CMIA (Model/Catalog Number: KR-β2-MG-01100C) is a medical device manufactured by Xiamen Innodx Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102039002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KR-β2-MG-01100C
Product Code / EMDN
W0102039002
Device Name
INNODX ß2-MG CMIA
Database Sync Date
2026-08-09 16:48:54

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 INNODX ß2-MG CMIA?

The registered manufacturer of record for INNODX ß2-MG CMIA is Xiamen Innodx Biotech Co., Ltd..

What is the Primary UDI-DI identifier for INNODX ß2-MG CMIA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-KR-B2-MG-01100CAV.

What classification code is assigned to this device?

This device is registered under product classification code W0102039002.

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