ReSolve ConvertX®

37 catalogue numbers from 00884450452851, listed by Merit Medical Systems, Inc., United States, under Stent, Ureteral. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
37catalogue 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 ReSolve ConvertX®
Listed by Merit Medical Systems, 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
Record published 2020-01-29
Record revised 2021-10-11 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Packaging Pack of 5

Catalogue Numbers

Catalogue numbers for ReSolve ConvertX®
Catalogue number Size Status
00884450452851 In distribution
00884450458549 In distribution
00884450453148 In distribution
00884450453186 In distribution
00884450453155 In distribution
00884450453094 In distribution
C In distribution
C In distribution
C In distribution
00884450721292 In distribution
C In distribution
00884450458488 In distribution
00884450458587 In distribution
00884450453032 In distribution
00884450458464 In distribution
00884450453124 In distribution
00884450452868 In distribution
00884450458563 In distribution
00884450721308 In distribution
00884450453193 In distribution
00884450458525 In distribution
00884450721537 In distribution
00884450721322 In distribution
00884450458501 In distribution
C In distribution
00884450458600 In distribution
C In distribution
00884450453070 In distribution
00884450721261 In distribution
00884450453179 In distribution
C In distribution
00884450453162 In distribution
C In distribution
00884450452875 In distribution
00884450453100 In distribution
00884450721193 In distribution
C 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