UltrafleX Quad

Ultraflex Quad High Fluid Cart With Smoke Evacuator

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (2), Shanghai (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code JCX
Manufacturer City Province Registered as Device types
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Jiangsu Jumao X-Care Medical Equipment Co., Ltd. Danyang Jiangsu Contract manufacturer 37
Laerdal Medical (Suzhou) Co., Ltd. 215009 Suzhou Jiangsu Province Repacker / relabeller 12
Vega Technologies Inc. Dongguan Guangdong Repacker / relabeller 7
Foshan Care Medical Technology Co., Ltd. Foshan Guangdong Manufacturer 3

Record

Regulatory record for UltrafleX Quad
Listed by Dornoch Medical Systems, United States
FDA product code JCX
Device type Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device class Class 2
Regulation 21 CFR 878.4780
510(k) K123188
Record published 2018-01-10
Record revised 2022-05-26 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries expiry date, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for UltrafleX Quad
Catalogue number Size Status
UL-QD500 In distribution
UL-QD500SE In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeVilbiss DeVilbiss Healthcare LLC. 35
Neptune Stryker GmbH 16
Apparatus, Suction, Ward Use, Portable, Ac-Powered Zimmer Orthopaedic Surgical Products 16
IntelliCart™ Zimmer Orthopaedic Surgical Products 13
Penumbra System Penumbra Inc. 8
Schuco Allied Medical LLC 7
Gomco Allied Medical LLC 7
Roscoe Medical Drive DeVilbiss Healthcare 5
Cliq Aspirator Anest Iwata Sparmax Co., Ltd. 5
Drive Drive DeVilbiss Healthcare 4
Truvic Generator Taiwan Biomaterial Company, Ltd. 4
Phantom Innovative Med, Inc. 4

Showing 12 of 65. All products under Apparatus, Suction, Ward Use, Portable, Ac-Powered

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190789 2019-04-24
K172481 2017-09-14
K162421 2016-12-21
K133786 2014-03-21
K123188 2013-03-04
K081047 2008-04-29

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer