GUDIDData
eudamed_udi Primary ID: D-CNMF000014455-BF-M227K

Unspecified Brand (UDI D-CNMF000014455-BF-M227K)

Manufactured by Wuxi Biohermes Bio & Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID D-CNMF000014455-BF-M227K

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: BF-M22) is a medical device manufactured by Wuxi Biohermes Bio & Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0201069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BF-M22
Product Code / EMDN
W0201069099
Device Name
Multi Function Immunofluorescence Analyzer
Database Sync Date
2026-08-09 16:48:23

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Wuxi Biohermes Bio & Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-CNMF000014455-BF-M227K.

What classification code is assigned to this device?

This device is registered under product classification code W0201069099.

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