Rempress

Nemoto Rempress contrast delivery system for angiography, pedestal type unit.

Registry build 21.09.26
15manufacturers in China registered for this device type
1catalogue number
7510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (7), Jiangsu (3), Shandong (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DXT
Manufacturer City Province Registered as Device types
Changzhou DSB Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 16
Hangzhou Jincheng Medical Supplies Manufacture Co., Ltd. Hangzhou Zhejiang Contract manufacturer 15
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
ShanDong WeiGao Group Medical Polymer Co., Ltd. Weihai Shandong Contract manufacturer 3
Jiangxi Baoeran Biomedical Science & Technology Co., Ltd. Fuzhou Jiangxi Contract manufacturer 1
Suzhou Meccan Import and Export Corp. Suzhou Jiangsu Contract manufacturer 71
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Wuxi Yushou Medical Appliances Co., Ltd. Wuxi Jiangsu Contract manufacturer 8
Shandong INT Medical Instruments Co., Ltd. Rizhao Shandong Manufacturer 4
Zhuhai DR Medical Instruments Co., Ltd. Zhuhai Guangdong Manufacturer 4
Shenzhen Antmed Co., Ltd. Dongguan Guangdong Manufacturer 4

Showing 12 of 15. All 15 manufacturers in China registered for Injector And Syringe, Angiographic

Record

Regulatory record for Rempress
Listed by Nemoto Kyorindo Co., Ltd., Japan
FDA product code DXT
Device type Injector And Syringe, Angiographic
Device class Class 2
Regulation 21 CFR 870.1650
Establishment Manufacturer
510(k) K092896
Record published 2016-07-15
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries serial number
Storage Storage environment atmospheric pressure 50 to 106 KiloPascal; Storage environment humidity 5 to 95 % RH; Storage environment temperature -40 to 70 °C
Packaging Carton

Catalogue Numbers

Catalogue numbers for Rempress
Catalogue number Size Status
100 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sinton Medical Products Shenzhen Boon Medical Supply Co., Ltd. 199
DeRoyal Deroyal Industries, Inc. 138
Antmed Shenzhen Antmed Co., Ltd. 91
Medline Industries, Inc. Medline Industries, Inc. 59
LF Liebel-Flarsheim Company LLC 58
Namic Medline Industries, Inc. 50
Merit Medical® Merit Medical Systems, Inc. 46
Medical Imaging Solutions International Shenzhen Boon Medical Supply Co., Ltd. 43
LF Shenzhen Boon Medical Supply Co., Ltd. 38
Namic Navilyst Medical, Inc. 38
Coeur Coeur, Inc. 38
Medical Imaging Solutions Intl. Medical Imaging Solutions, Inc. 37

Showing 12 of 168. All products under Injector And Syringe, Angiographic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242212 2024-08-27
K173450 2018-02-07
K133189 2014-06-30
K092896 2010-10-29
K071691 2007-12-19
K062168 2006-08-18
K052633 2005-10-17

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