Merit Pursue™

15 catalogue numbers from 00884450358689, listed by Merit Medical Systems, Inc., United States, under Catheter, Percutaneous. 14 manufacturers in China are registered for this product code.

Registry build 21.09.26
14manufacturers in China registered for this device type
15catalogue numbers in this listing
6510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Shanghai (5), Jiangsu (5), Guangdong (3). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQY
Manufacturer City Province Registered as Device types
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Covidien Medical Products (Shanghai) Manufacturing LLC Shanghai Shanghai Contract manufacturer 8
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Showing 12 of 14. All 14 manufacturers in China registered for Catheter, Percutaneous

Record

Regulatory record for Merit Pursue™
Listed by Merit Medical Systems, Inc., United States
FDA product code DQY
Device type Catheter, Percutaneous
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2019-01-16
Record revised 2021-10-11 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Packaging Pack of 20

Catalogue Numbers

Catalogue numbers for Merit Pursue™
Catalogue number Size Status
00884450358689 Catheter Length-110 cm (43″) In distribution
00884450358535 Catheter Tip Shape-Straight In distribution
00884450358733 Catheter Tip Shape-Swan Neck In distribution
00884450358726 Catheter Tip Shape-45° In distribution
00884450358498 Catheter Tip Shape-Swan Neck In distribution
00884450358665 Catheter Length-110 cm (43″) In distribution
00884450358740 Catheter Length-150 cm (59″) In distribution
00884450358672 Catheter Tip Shape-Swan Neck In distribution
00884450358481 Distal French Size (F)-1.7F In distribution
00884450358559 Distal French Size (F)-1.7F In distribution
00884450358566 Catheter Tip Shape-Straight In distribution
00884450358719 Catheter Tip Shape-Straight In distribution
00884450358542 Catheter Length-150 cm (59″) In distribution
00884450358528 Catheter Tip Shape-Swan Neck In distribution
00884450358504 Catheter Tip Shape-Straight In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Launcher™ Medtronic, Inc. 3,805
Sherpa NX Balanced™ Medtronic, Inc. 1,523
Arrow Teleflex Medical LLC 1,249
Z2 Medtronic, Inc. 955
Vista Brite TIP Cordis Corp. 789
Mach1™ Boston Scientific Corporation 777
Sherpa NX Active Medtronic, Inc. 571
Zuma® Medtronic, Inc. 569
Convey Pendracare International B.V. 532
Taiga Medtronic, Inc. 307
RunWay™ Boston Scientific Corporation 300
ConcierGE Guiding Excellence™ Merit Medical Systems, Inc. 295

Showing 12 of 500. All products under Catheter, Percutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242873 2025-01-15
K231246 2023-08-30
K202610 2020-12-14
K173548 2018-03-30
K132409 2013-08-29
K121051 2012-06-13

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of Merit Pursue™
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Merit Medical Systems, Inc. UDI-DI 2023-11-06 Class II Package design/selection The sterility of microcatheter and infusion system devices cannot be guaranteed. 59 units

Recalls

The FDA has not published a severity grade for these. 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
2010-12-16 Not classified Packaging process control Compromised sterility/weak or open seals. 28,679 for all products 2012-08-08
2004-10-15 Not classified Other Merit Safety Paracentesis Procedure Trays contain Monoject Magellan safety needles which have been recalled by Tyco Healthcare.These needles may detach from their hub during use. 2141 trays 2004-12-15

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