ReSolve®

24 catalogue numbers from 00884450313299, listed by Merit Medical Systems, Inc., United States, under Stents, Drains And Dilators For The Biliary Ducts. 6 manufacturers in China are registered for this product code.

Registry build 21.09.26
6manufacturers in China registered for this device type
24catalogue numbers in this listing
5510(k) clearances naming this product code
11recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Zhejiang (2), Guangdong (1).

Chinese manufacturers registered for FDA product code FGE
Manufacturer City Province Registered as Device types
Micro-Tech (Nanjing) Co., Ltd. Nan Jing Jiangsu Contract manufacturer 49
Zhejiang Chuangxiang Medical Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 27
Jiangsu Vedkang Medical Science and Technology Co., Ltd. Changzhou Jiangsu Manufacturer 20
Hangzhou AGS MedTech Co., Ltd. Hangzhou Zhejiang Repacker / relabeller 19
Dongguan TT Medical, Inc. Dongguan Guangdong Manufacturer 4
LEO Medical Co., Ltd. Changzhou Jiangsu Manufacturer 4

Record

Regulatory record for ReSolve®
Listed by Merit Medical Systems, Inc., United States
FDA product code FGE
Device type Stents, Drains And Dilators For The Biliary Ducts
Device class Class 2
Regulation 21 CFR 876.5010
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2017-07-05
Record revised 2024-10-14 (version 5)

Specifications

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

Catalogue Numbers

Catalogue numbers for ReSolve®
Catalogue number Size Status
00884450313299 Pigtail To Marker Band-11 cm In distribution
00884450683903 Catheter Length (cm)-40 cm In distribution
00884450683927 Catheter Length (cm)-40 cm In distribution
00884450685129 French Size (F)-10F In distribution
00884450683910 Catheter Length (cm)-40 cm In distribution
00884450313282 Pigtail To Marker Band-11 cm In distribution
00884450012826 Pigtail To Marker Band-14 cm In distribution
00884450685150 French Size (F)-8.5F In distribution
00884450012796 French Size (F)-8.5F In distribution
00884450313244 Catheter Length (cm)-40 cm In distribution
00884450313237 Catheter Length (cm)-40 cm In distribution
00884450057537 Catheter Length (cm)-40 cm In distribution
00884450313305 Pigtail To Marker Band-11 cm In distribution
00884450313251 Catheter Length (cm)-40 cm In distribution
00884450685136 Pigtail To Marker Band-11 cm In distribution
00884450313268 Catheter Length (cm)-40 cm In distribution
00884450057506 French Size (F)-12F In distribution
00884450057476 Pigtail To Marker Band-11 cm In distribution
00884450683897 Catheter Length (cm)-40 cm In distribution
00884450012819 Catheter Length (cm)-40 cm In distribution
00884450057568 Pigtail To Marker Band-11 cm In distribution
00884450012802 Catheter Length (cm)-40 cm In distribution
00884450313275 French Size (F)-10F In distribution
00884450685143 French Size (F)-14F In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Zimmon Cook Ireland Ltd 213
Single Use Biliary Drainage Stent V Olympus Medical Systems Corp. 181
Mustang™ Boston Scientific Corporation 167
Geenen Cook Ireland Ltd 158
Cotton-Leung Cook Ireland Ltd 144
Advanix™ Pancreatic Stent Boston Scientific Corporation 135
Single Use Biliary Stent V Olympus Medical Systems Corp. 106
Single-use Balloon Dilatation Catheter LEO Medical Co., Ltd. 102
Biliary Plastic Stent Set Micro-Tech (Nanjing) Co., Ltd. 90
Biliary Plastic Stent Micro-Tech (Nanjing) Co., Ltd. 90
M-Drain Mermaid Medical A/S 86
Advanix™ Biliary Boston Scientific Corporation 84

Showing 12 of 212. All products under Stents, Drains And Dilators For The Biliary Ducts

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K151925 2015-11-06
K141408 2014-11-26
K121832 2012-07-17
K093947 2010-01-21
K063733 2007-11-14

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2013-01-16 Class II Nonconforming Material/Component A consumer complaint that a catheter was observed to be in several pieces under patient fluoroscopic visualization. 387 units 2015-09-16
2010-01-28 Not classified Component change control Degradation of the outer portion of the delivery catheter may prevent proper deployment of the biliary stent. 69 units 2010-04-27
2010-01-28 Not classified Component change control Degradation of the outer portion of the delivery catheter may prevent proper deployment of the biliary stent. 16 units 2010-04-27
2010-01-28 Not classified Component change control Degradation of the outer portion of the delivery catheter may prevent proper deployment of the biliary stent. 8 units 2010-04-27
2010-01-28 Not classified Component change control Degradation of the outer portion of the delivery catheter may prevent proper deployment of the biliary stent. 15 units 2010-04-27
2010-01-28 Not classified Component change control Degradation of the outer portion of the delivery catheter may prevent proper deployment of the biliary stent. 51 units 2010-04-27
2010-01-28 Not classified Component change control Degradation of the outer portion of the delivery catheter may prevent proper deployment of the biliary stent. 6 units 2010-04-27
2008-11-07 Not classified Other Biliary drainage catheter tips may separate from the catheter shaft after placement. 108 units 2009-08-05
2008-11-07 Not classified Other Biliary drainage catheter tips may separate from the catheter shaft after placement. 284 units 2009-08-05
2008-11-07 Not classified Other Biliary drainage catheter tips may separate from the catheter shaft after placement. 528 units 2009-08-05
2008-11-07 Not classified Other Biliary drainage catheter tips may separate from the catheter shaft after placement. 244 units 2009-08-05

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