Double-J

8.5FR(2.81mm) X 30 cm SURGITEK DOUBLE-J CLOSED TIP URETERAL STENT

Registry build 21.09.26
4manufacturers in China registered for this device type
23catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code FAD
Manufacturer City Province Registered as Device types
Zhejiang Chuangxiang Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Alton Shanghai Medical Instruments Co Ltd Shanghai Shanghai Complaint-file establishment 20
BQ Plus Medical Co., Ltd. Songjiang Shanghai Contract manufacturer 13
Shenzhen Trious Medical Technology Co., Ltd. Shenzhen Guangdong Manufacturer 6

Record

Regulatory record for Double-J
Listed by Gyrus Acmi, Inc., United States
FDA product code FAD
Device type Stent, Ureteral
Device class Class 2
Regulation 21 CFR 876.4620
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K781641
Record published 2015-10-24
Record revised 2024-09-02 (version 5)

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

Catalogue Numbers

Catalogue numbers for Double-J
Catalogue number Size Status
5209400 In distribution
5209200 In distribution
5202100 In distribution
5204700 In distribution
5203600 In distribution
5202200 In distribution
5209800 In distribution
5209100 In distribution
5202800 In distribution
5202600 In distribution
5202000 In distribution
5208600 In distribution
5202400 In distribution
5204100 In distribution
5201800 In distribution
5204400 In distribution
5209000 In distribution
5202700 In distribution
5204800 In distribution
5204200 In distribution
5204600 In distribution
5209050 In distribution
5209600 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Porges Coloplast Coloplast A/S 509
Polaris™ Ultra Boston Scientific Corporation 406
Universa Cook Incorporated 384
Percuflex™ Plus Boston Scientific Corporation 300
Polaris™ Loop Boston Scientific Corporation 232
ImaJin Coloplast A/S 219
Contour™ Boston Scientific Corporation 205
Percuflex™ Boston Scientific Corporation 152
Tecoflex Gyrus Acmi, Inc. 92
Vortek Coloplast A/S 92
Sof-Flex Cook Incorporated 60
Tria™ Firm Boston Scientific Corporation 58

Showing 12 of 131. All products under Stent, Ureteral

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