Mustang™

167 catalogue numbers from H74939171050340, listed by Boston Scientific Corporation, 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
167catalogue numbers in this listing
56510(k) clearances naming this product code
40recalls 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 Mustang™
Listed by Boston Scientific Corporation, 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 Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-08-04
Record revised 2019-08-09 (version 3)

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 Mustang™
Catalogue number Size Status
H74939171050340 30 mm Length In distribution
H74939171060640 60 mm Length In distribution
H74939171080440 40 mm Length In distribution
H74939171100210 10.0 mm Diameter In distribution
H74939171030640 60 mm Length In distribution
H74939171100410 135 cm Effective Length In distribution
H74939171080840 40 cm Effective Length In distribution
H74939171090410 9.0 mm Diameter In distribution
H74939171090310 9.0 mm Diameter In distribution
H74939171050840 5.0 mm Diameter In distribution
H74939171100610 10.0 mm Diameter In distribution
H74939171061040 6.0 mm Diameter In distribution
H74939171080340 8.0 mm Diameter In distribution
H74939171040840 40 cm Effective Length In distribution
H74939171050410 40 mm Length In distribution
H74939171100270 75 cm Effective Length In distribution
H74939171120410 40 mm Length In distribution
H74939171050670 75 cm Effective Length In distribution
H74939171050610 60 mm Length In distribution
H74939171060410 40 mm Length In distribution
H74939171080310 8.0 mm Diameter In distribution
H74939171080270 8.0 mm Diameter In distribution
H74939171070210 20 mm Length In distribution
H74939171090340 40 cm Effective Length In distribution
H74939171070410 40 mm Length In distribution
H74939171061010 6.0 mm Diameter In distribution
H74939171081270 75 cm Effective Length In distribution
H74939171070610 60 mm Length In distribution
H74939171061210 135 cm Effective Length In distribution
H74939171060870 80 mm Length In distribution
H74939171070810 135 cm Effective Length In distribution
H74939171071270 120 mm Length In distribution
H74939171040340 40 cm Effective Length In distribution
H74939171040270 20 mm Length In distribution
H74939171100810 10.0 mm Diameter In distribution
H74939171090370 30 mm Length In distribution
H74939171120210 12.0 mm Diameter In distribution
H74939171030470 40 mm Length In distribution
H74939171060610 6.0 mm Diameter In distribution
H74939171120870 75 cm Effective Length In distribution
H74939171061270 75 cm Effective Length In distribution
H74939171031270 75 cm Effective Length In distribution
H74939171100310 135 cm Effective Length In distribution
H74939171070370 30 mm Length In distribution
H74939171030310 30 mm Length In distribution
H74939171120370 12.0 mm Diameter In distribution
H74939171100470 40 mm Length In distribution
H74939171040670 60 mm Length In distribution
H74939171080240 40 cm Effective Length In distribution
H74939171100370 75 cm Effective Length In distribution
H74939171050310 30 mm Length In distribution
H74939171090670 9.0 mm Diameter In distribution
H74939171060210 20 mm Length In distribution
H74939171060340 40 cm Effective Length In distribution
H74939171120840 40 cm Effective Length In distribution
H74939171100640 10.0 mm Diameter In distribution
H74939171120340 30 mm Length In distribution
H74939171040410 135 cm Effective Length In distribution
H74939171120240 20 mm Length In distribution
H74939171090640 9.0 mm Diameter In distribution
H74939171050440 40 cm Effective Length In distribution
H74939171081040 40 cm Effective Length In distribution
H74939171120470 12.0 mm Diameter In distribution
H74939171080370 75 cm Effective Length In distribution
H74939171100670 75 cm Effective Length In distribution
H74939171071040 40 cm Effective Length In distribution
H74939171070340 30 mm Length In distribution
H74939171080210 20 mm Length In distribution
H74939171070840 80 mm Length In distribution
H74939171100340 10.0 mm Diameter In distribution
H74939171080670 75 cm Effective Length In distribution
H74939171090810 80 mm Length In distribution
H74939171030670 3.0 mm Diameter In distribution
H74939171051070 100 mm Length In distribution
H74939171070270 75 cm Effective Length In distribution
H74939171120440 40 mm Length In distribution
H74939171030340 30 mm Length In distribution
H74939171030210 20 mm Length In distribution
H74939171050810 135 cm Effective Length In distribution
H74939171071210 7.0 mm Diameter In distribution
H74939171030810 80 mm Length In distribution
H74939171060470 75 cm Effective Length In distribution
H74939171041210 120 mm Length In distribution
H74939171090440 40 mm Length In distribution
H74939171040810 80 mm Length In distribution
H74939171051240 5.0 mm Diameter In distribution
H74939171031210 3.0 mm Diameter In distribution
H74939171080470 40 mm Length In distribution
H74939171030440 40 cm Effective Length In distribution
H74939171081070 8.0 mm Diameter In distribution
H74939171120670 60 mm Length In distribution
H74939171120810 135 cm Effective Length In distribution
H74939171090870 9.0 mm Diameter In distribution
H74939171031010 3.0 mm Diameter In distribution
H74939171050240 40 cm Effective Length In distribution
H74939171070470 75 cm Effective Length In distribution
H74939171050370 75 cm Effective Length In distribution
H74939171070640 40 cm Effective Length In distribution
H74939171120640 60 mm Length In distribution
H74939171090210 9.0 mm Diameter In distribution
H74939171060370 30 mm Length In distribution
H74939171090470 9.0 mm Diameter In distribution
H74939171120270 12.0 mm Diameter In distribution
H74939171100870 80 mm Length In distribution
H74939171060840 6.0 mm Diameter In distribution
H74939171051040 5.0 mm Diameter In distribution
H74939171030240 20 mm Length In distribution
H74939171120610 12.0 mm Diameter In distribution
H74939171041010 4.0 mm Diameter In distribution
H74939171041270 120 mm Length In distribution
H74939171050870 80 mm Length In distribution
H74939171051010 100 mm Length In distribution
H74939171040240 40 cm Effective Length In distribution
H74939171080640 8.0 mm Diameter In distribution
H74939171041040 100 mm Length In distribution
H74939171050470 75 cm Effective Length In distribution
H74939171030870 3.0 mm Diameter In distribution
H74939171071010 7.0 mm Diameter In distribution
H74939171090240 20 mm Length In distribution
H74939171040440 40 mm Length In distribution
H74939171030840 40 cm Effective Length In distribution
H74939171060310 30 mm Length In distribution
H74939171060240 6.0 mm Diameter In distribution
H74939171070240 20 mm Length In distribution
H74939171031040 3.0 mm Diameter In distribution
H74939171090270 75 cm Effective Length In distribution
H74939171080610 8.0 mm Diameter In distribution
H74939171070440 7.0 mm Diameter In distribution
H74939171100440 40 mm Length In distribution
H74939171090610 60 mm Length In distribution
H74939171030270 20 mm Length In distribution
H74939171040610 60 mm Length In distribution
H74939171080410 8.0 mm Diameter In distribution
H74939171080870 8.0 mm Diameter In distribution
H74939171060670 75 cm Effective Length In distribution
H74939171061070 75 cm Effective Length In distribution
H74939171050210 5.0 mm Diameter In distribution
H74939171070670 60 mm Length In distribution
H74939171040370 4.0 mm Diameter In distribution
H74939171060440 40 cm Effective Length In distribution
H74939171041070 75 cm Effective Length In distribution
H74939171030410 3.0 mm Diameter In distribution
H74939171100840 40 cm Effective Length In distribution
H74939171051210 120 mm Length In distribution
H74939171040210 4.0 mm Diameter In distribution
H74939171081010 100 mm Length In distribution
H74939171081210 135 cm Effective Length In distribution
H74939171051270 75 cm Effective Length In distribution
H74939171070870 80 mm Length In distribution
H74939171070310 30 mm Length In distribution
H74939171031070 75 cm Effective Length In distribution
H74939171040640 40 cm Effective Length In distribution
H74939171061240 120 mm Length In distribution
H74939171040470 40 mm Length In distribution
H74939171080810 80 mm Length In distribution
H74939171040870 80 mm Length In distribution
H74939171030370 75 cm Effective Length In distribution
H74939171040310 4.0 mm Diameter In distribution
H74939171050640 40 cm Effective Length In distribution
H74939171071070 7.0 mm Diameter In distribution
H74939171050270 5.0 mm Diameter In distribution
H74939171060810 135 cm Effective Length In distribution
H74939171030610 60 mm Length In distribution
H74939171120310 12.0 mm Diameter In distribution
H74939171060270 20 mm Length In distribution
H74939171090840 40 cm Effective Length In distribution
H74939171100240 20 mm Length 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
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
Visi-Pro™ Covidien LP 81

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
K251291 2025-07-03
K242950 2024-12-06
K240464 2024-08-30
K223469 2023-06-15
K223592 2022-12-29
K203162 2020-12-18
K172520 2017-10-04
K171809 2017-08-09
K162404 2016-10-12
K152853 2015-11-20
K152607 2015-10-27
K141335 2014-10-17
K141597 2014-08-22
K133110 2014-07-02
K140630 2014-05-23
K133700 2014-05-14
K130484 2013-08-09
K122072 2012-09-28
K112994 2012-02-10
K112543 2011-12-29
K112701 2011-10-25
K110122 2011-05-12
K102082 2010-08-23
K101314 2010-07-23
K101786 2010-07-23
K083374 2009-04-22
K083627 2009-04-07
K081733 2008-10-27
K061231 2006-09-01
K041606 2004-07-07
K040027 2004-03-30
K032025 2003-09-25
K032360 2003-08-27
K030645 2003-03-25
K030107 2003-03-21
K021630 2002-10-25
K011909 2001-11-28
K012752 2001-11-15
K003929 2001-03-22
K002133 2000-10-12
K001338 2000-08-30
K000308 2000-05-19
K993303 2000-03-23
K982508 1998-10-16
K973008 1997-12-15
K973113 1997-11-10
K965147 1997-06-30
K963254 1997-05-21
K962899 1997-05-20
K970052 1997-03-25
K963691 1996-12-12
K963397 1996-11-25
K930623 1994-09-28
K924608 1994-01-26
K900205 1991-08-20
K910931 1991-04-02

Recalls

39 of these are 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
2026-05-21 Class II Package design/selection Potential sterile breach of the pouches in which devices are packaged. 81,543 units
2026-05-21 Class II Package design/selection Potential sterile breach of the pouches in which devices are packaged. 81,543 units
2026-05-21 Class II Package design/selection Potential sterile breach of the pouches in which devices are packaged. 81,543 units
2026-05-21 Class II Package design/selection Potential sterile breach of the pouches in which devices are packaged. 81,543 units
2026-05-21 Class II Package design/selection Potential sterile breach of the pouches in which devices are packaged. 81,543 units
2026-05-21 Class II Package design/selection Potential sterile breach of the pouches in which devices are packaged. 81,543 units
2025-08-28 Class II Process control The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa. 156 units
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2021-10-21 Class II Device Design Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
2020-09-16 Class II Vendor change control RX tunnel component (black sheath) may detach from the catheter shaft due to lower bond strength. 15,062 devices distributed in US. 12,930 distributed OUS
2020-08-07 Class II Packaging process control Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices labeled as
WallFlexTM Biliary RX Fully Covered Stent System RMV 10x60mm device
40 units 2020-12-23
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 139 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 66 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 271 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 940 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 109 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 35 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 66 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 542 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 97 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 54 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 222 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 179 units 2023-12-20
2019-10-21 Class II Incorrect or no expiration date Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life 651 units 2023-12-20
2018-12-26 Class II Other The sterile barrier may contain packaging seal
defects.
75 units 2020-04-17
2018-12-26 Class II Other The sterile barrier may contain packaging seal
defects.
18 units 2020-04-17
2017-06-01 Class II Employee error Label on the affected devices incorrectly identifies the
injection location as “above” the balloon when it should be below the balloon and “below” the balloon when it should be above the balloon
32 units 2018-06-26
2017-06-01 Class II Employee error Label on the affected devices incorrectly identifies the
injection location as “above” the balloon when it should be below the balloon and “below” the balloon when it should be above the balloon
39 units 2018-06-26
2015-04-27 Class II Employee error One lot of the Extractor” Pro RX Retrieval Balloon Catheter (9-12mm balloon) contains an incorrect syringe size (12-15mm), which is larger than the size identified on the label. 39 units 2016-01-27
2015-02-25 Class II Device Design Complaints of device fragmentation after the catheter was implanted in the biliary system. The most serious patient risk for this issue is additional intervention for fragment retrieval using minimally invasive methods and, in some of the r 289 2017-06-30
2015-02-25 Class II Nonconforming Material/Component Boston Scientific is initiating this Medical Device Field Correction of the Expel” APD and APDL
Drainage Catheters. To date, Boston Scientific has received one complaint for device fragmentation
after an Expel” APD catheter was implanted in
918 2016-08-12
2013-12-18 Class II Process control Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size 39 units 2014-08-19
2013-12-18 Class II Process control Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive hole location or balloon size 38 units 2014-08-19
2010-02-18 Not classified Packaging Boston Scientific Corporation is conducting a Medical Device Recall Removal of specific lots/batches of the Blue Max and Ultrathin Diamond Balloon Dilatation Catheters. Boston Scientific has determined that, the sterile barrier in the cathe 99 2011-12-10

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