GUDIDData
eudamed_udi Primary ID: 04710469879005

Clever Check Lantete sterile pentru (UDI 04710469879005)

Manufactured by TaiDoc Technology Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Clever Check Lantete sterile pentru - Primary ID 04710469879005

Device Regulatory Overview

The Clever Check Lantete sterile pentru (Model/Catalog Number: TD-5084) is a medical device manufactured by TaiDoc Technology Corporation. This product is indexed under FDA Product Code / Category Classification V010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TD-5084
Product Code / EMDN
V010402
Device Name
Blood Lancet
Database Sync Date
2026-08-09 16:29:18

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 Clever Check Lantete sterile pentru?

The registered manufacturer of record for Clever Check Lantete sterile pentru is TaiDoc Technology Corporation.

What is the Primary UDI-DI identifier for Clever Check Lantete sterile pentru?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04710469879005.

What classification code is assigned to this device?

This device is registered under product classification code V010402.

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