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eudamed_udi Primary ID: 19120049207692

MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, paper label, pre-assembled with Carrier T (UDI 19120049207692)

Manufactured by Greiner Bio-One GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, paper label, pre-assembled with Carrier T - Primary ID 19120049207692

Device Regulatory Overview

The MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, paper label, pre-assembled with Carrier T (Model/Catalog Number: 450562) is a medical device manufactured by Greiner Bio-One GmbH. This product is indexed under FDA Product Code / Category Classification W0501010203 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0802-2025 View Full Alert →

VACUETTE SAFELINK, REF: 450210...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
450562
Product Code / EMDN
W0501010203
Device Name
MiniCollect® FX Sodium Fluoride / Potassium Oxalate TUBE
Database Sync Date
2026-08-09 16:48:53

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 MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, paper label, pre-assembled with Carrier T?

The registered manufacturer of record for MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, paper label, pre-assembled with Carrier T is Greiner Bio-One GmbH.

What is the Primary UDI-DI identifier for MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, paper label, pre-assembled with Carrier T?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 19120049207692.

What classification code is assigned to this device?

This device is registered under product classification code W0501010203.

Similar Classification Devices (W0501010203)

Other Devices by Greiner Bio-One GmbH

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