Vacuum Pump Tubing

3 catalogue numbers from 14211, listed by Vitrolife Sweden AB, Sweden, under Needle, Assisted Reproduction. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

All of them in Guangdong.

Chinese manufacturers registered for FDA product code MQE
Manufacturer City Province Registered as Device types
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Shenzhen VitaVitro Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 7
Gimbo Medical Technology Shenzhen Co., Ltd. Shenzhen Guangdong Manufacturer 3

Record

Regulatory record for Vacuum Pump Tubing
Listed by Vitrolife Sweden AB, Sweden
FDA product code MQE
Device type Needle, Assisted Reproduction
Device class Class 2
Regulation 21 CFR 884.6100
Establishment Manufacturer
510(k) K991273
Record published 2016-09-14
Record revised 2021-12-07 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Distribution end date 2021-12-06

Catalogue Numbers

Catalogue numbers for Vacuum Pump Tubing
Catalogue number Size Per pack Status
14211 10 Withdrawn
14205 10 Withdrawn
14212 10 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cook William A. Cook Australia PTY, Ltd. 71
Follicle Aspiration Set Single Lumen Vitrolife Sweden AB 40
Follicle Aspiration Set, Double Lumen Vitrolife Sweden AB 28
Wallace ICU Medical, Inc 20
Kitazato OPU Needle with Connection Tube, Type2-v17 Kitazato Corporation 18
Labotect Labotect Labor-Technik Göttingen Gesellschaft mit beschränkter Haftung 16
Kitazato OPU Needle Kitazato Corporation 12
Follicle Aspiration Set Reduced Single Lumen Vitrolife Sweden AB 11
Follicle Aspiration Set Single Lumen, Luer Vitrolife Sweden AB 9
Needle Guide Civco Medical Instruments Co., Inc. 8
17G Wallace Dual Lumen Oocyte Recovery Set Coopersurgical, Inc. 3
ACE-M Allwin Medical Devices, Inc. 3

Showing 12 of 65. All products under Needle, Assisted Reproduction

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K172050 2017-11-21
K161970 2017-06-14
K082727 2009-02-06

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