GUDIDData
eudamed_udi Primary ID: 06958982140068

Blood Glucose Test Meters (UDI 06958982140068)

Manufactured by Abiores Technology (Beijing) Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Blood Glucose Test Meters - Primary ID 06958982140068

Device Regulatory Overview

The Blood Glucose Test Meters (Model/Catalog Number: S9155) is a medical device manufactured by Abiores Technology (Beijing) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0201060102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S9155
Product Code / EMDN
W0201060102
Device Name
Blood Glucose Test Meters
Database Sync Date
2026-08-09 16:45:48

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 Blood Glucose Test Meters?

The registered manufacturer of record for Blood Glucose Test Meters is Abiores Technology (Beijing) Co.,Ltd..

What is the Primary UDI-DI identifier for Blood Glucose Test Meters?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140068.

What classification code is assigned to this device?

This device is registered under product classification code W0201060102.

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