GUDIDData
gudid Primary ID: 6890365

Drawer for Low mobile carts (UDI 6890365)

Manufactured by Maquet Critical Care AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Drawer for Low mobile carts - Primary ID 6890365

Device Regulatory Overview

The Drawer for Low mobile carts (Model/Catalog Number: 6890365) is a medical device manufactured by Maquet Critical Care AB. This product is indexed under FDA Product Code / Category Classification CBK within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2014-2025 View Full Alert →

Servo-n Ventilator System. Model Number: 6694800....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2013-2025 View Full Alert →

Servo-u Ventilator System. Model Number: 6688600....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2015-2025 View Full Alert →

Servo-u MR Ventilator System. Model Number: 6888800....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
6890365
Product Code / EMDN
CBK
Device Name
Database Sync Date
2026-08-09 09:10:28

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 Drawer for Low mobile carts?

The registered manufacturer of record for Drawer for Low mobile carts is Maquet Critical Care AB.

What is the Primary UDI-DI identifier for Drawer for Low mobile carts?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6890365.

What classification code is assigned to this device?

This device is registered under product classification code CBK.

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