GUDIDData
eudamed_udi Primary ID: 04710469878961

XPER Technology Blood Glucose Test Strips(50pcs/Box)(Procheck Advance) (UDI 04710469878961)

Manufactured by TaiDoc Technology Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for XPER Technology Blood Glucose Test Strips(50pcs/Box)(Procheck Advance) - Primary ID 04710469878961

Device Regulatory Overview

The XPER Technology Blood Glucose Test Strips(50pcs/Box)(Procheck Advance) (Model/Catalog Number: TD-4335) is a medical device manufactured by TaiDoc Technology Corporation. This product is indexed under FDA Product Code / Category Classification W0101060101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TD-4335
Product Code / EMDN
W0101060101
Device Name
Blood Glucose Test Strip
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 XPER Technology Blood Glucose Test Strips(50pcs/Box)(Procheck Advance)?

The registered manufacturer of record for XPER Technology Blood Glucose Test Strips(50pcs/Box)(Procheck Advance) is TaiDoc Technology Corporation.

What is the Primary UDI-DI identifier for XPER Technology Blood Glucose Test Strips(50pcs/Box)(Procheck Advance)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04710469878961.

What classification code is assigned to this device?

This device is registered under product classification code W0101060101.

Programmatic Export

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

JSON API Endpoint