GUDIDData
eudamed_udi Primary ID: 06975984064284

BNP (eCLIA) (UDI 06975984064284)

Manufactured by Shenzhen Lifotronic Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BNP (eCLIA) - Primary ID 06975984064284

Device Regulatory Overview

The BNP (eCLIA) (Model/Catalog Number: 0320511102) is a medical device manufactured by Shenzhen Lifotronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0320511102
Product Code / EMDN
W01021301
Device Name
BNP (eCLIA)
Database Sync Date
2026-08-09 16:51:58

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 BNP (eCLIA)?

The registered manufacturer of record for BNP (eCLIA) is Shenzhen Lifotronic Technology Co., Ltd..

What is the Primary UDI-DI identifier for BNP (eCLIA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975984064284.

What classification code is assigned to this device?

This device is registered under product classification code W01021301.

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