LF

60mL Dual MR Syringe with Single Check Valve Y Tubing (90"/2300mm) and Filling Spikes; fits injectors: OptiStar Elite and OptiStar LE

Registry build 21.09.26
15manufacturers in China registered for this device type
38catalogue numbers in this listing
3510(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 LF
Listed by Shenzhen Boon Medical Supply Co., Ltd., China
FDA product code DXT
Device type Injector And Syringe, Angiographic
Device class Class 2
Regulation 21 CFR 870.1650
Establishment Manufacturer
510(k) K182289
Record published 2020-01-18
Record revised 2020-06-01 (version 7)

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, manufacturing date
Packaging Carton of 50, carton of 20, carton of 5, box of 50, carton of 2, box of 20

Catalogue Numbers

Catalogue numbers for LF
Catalogue number Size Status
100104-S In distribution
100114-B In distribution
100104-S In distribution
100104-C In distribution
700103 In distribution
300103 In distribution
100114-C In distribution
200103-A In distribution
400202-1 In distribution
600102-3 In distribution
100114-D In distribution
700103 In distribution
400102-3 In distribution
600102-3 In distribution
300112-A In distribution
100104-A In distribution
400201-7 In distribution
600202-4 In distribution
400201-1 In distribution
100104-A In distribution
100104-D In distribution
300103-A In distribution
100104-C In distribution
300103 In distribution
200103-C In distribution
100104-N In distribution
200103-A In distribution
100114-A In distribution
100114-D In distribution
100104-D In distribution
100114-B In distribution
100104-B In distribution
100114-C In distribution
400102-3 In distribution
200103-C In distribution
100114-A In distribution
100104-B In distribution
300103-A 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
Namic Navilyst Medical, Inc. 38
Coeur Coeur, Inc. 38
Medical Imaging Solutions Intl. Medical Imaging Solutions, Inc. 37
CVi® Cable Acist Medical Systems, Inc. 30

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
K241109 2024-08-22
K211564 2021-10-19
K192657 2020-08-07

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