gudid Primary ID: 455052

VACUETTE (UDI 455052)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The VACUETTE (Model/Catalog Number: 455052) is a medical device manufactured by Greiner Bio-One GmbH. This product is indexed under FDA Product Code / Category Classification LIO 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

Verify if facility inventory is affected by this recall.

Unlock Lot Data ($49)

Technical Specifications

Model Number: 455052
Product Code / EMDN: LIO
Device Name: VACUETTE TUBE 10 ml Urine CCM 16x100 yellow cap-black ring, Round Base, non-ridged
Database Sync Date: 2026-08-09 10:01:32

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 VACUETTE?

The registered manufacturer of record for VACUETTE is Greiner Bio-One GmbH.

What is the Primary UDI-DI identifier for VACUETTE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 455052.

What classification code is assigned to this device?

This device is registered under product classification code LIO.

Similar Classification Devices (LIO)

Other Devices by Greiner Bio-One GmbH

Programmatic Export

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

JSON API Endpoint