Squirt®

Squirt®: 1 catalogue number listed by Merit Medical Systems, Inc., United States, under Catheter, Continuous Flush. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
7510(k) clearances naming this product code
27recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Shanghai (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KRA
Manufacturer City Province Registered as Device types
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3
Vascupatent Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 1

Record

Regulatory record for Squirt®
Listed by Merit Medical Systems, Inc., United States
FDA product code KRA
Device type Catheter, Continuous Flush
Device class Class 2
Regulation 21 CFR 870.1210
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2025-04-21

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
Packaging Pack of 5

Catalogue Numbers

Catalogue numbers for Squirt®
Catalogue number Size Status
A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fountain® Merit Medical Systems, Inc. 154
PulseSpray AngioDynamics, Inc. 149
Merit Maestro® Merit Medical Systems, Inc. 143
Phenom™ Catheter Cathera, Inc. 103
UniFuse AngioDynamics, Inc. 84
CXI Cook Incorporated 48
Uni-Fuse+ AngioDynamics, Inc. 32
Prowler Medos International Sàrl 27
Truwave, Vamp Edwards Lifesciences Technology Sarl 26
ICU Medical ICU Medical, Inc 21
Cantata Cook Incorporated 20
Truwave, Vamp Plus Edwards Lifesciences Technology Sarl 19

Showing 12 of 149. All products under Catheter, Continuous Flush

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211525 2021-07-16
K193082 2020-08-07
K201907 2020-08-06
K172081 2017-08-04
K161921 2016-11-04
K082613 2008-12-30
K962129 1997-04-15

Recalls

3 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
2023-11-06 Class II Package design/selection The sterility of microcatheter and infusion system devices cannot be guaranteed. 717 units
2014-09-26 Class II Mixed-up of materials/components These microcatheters were packaged with a 2.8 F distal tip, rather than the labeled 2.4 F. 56 units 2014-11-19
2013-12-06 Class II Packaging process control Merit Medical Systems, Inc. is conducting a recall for 3 lots of Maestro Microcatheters with a graphic
discrepancy on the carton/box label end panel. The catheter graphic on the front of the carton
box (correct) and the graphic on the end p
59 2014-01-27
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 40 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 19 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 5 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 240 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 44 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 42 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 18 uinits 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 240 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 10 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 5 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 5 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 149 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 59 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 370 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 5 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 11 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 5 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 29 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 7 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 31 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 4 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 26 units 2010-09-13
2010-01-06 Not classified Storage Infusion catheters may become brittle and break during use. 25 units 2010-09-13
2008-05-14 Not classified Packaging process control Catheters were packaged with occluding wires that were too long for the catheter. Potential for wire to not occlude the catheter appropriately, allowing the wire to exit the tip of the catheter further than intended, posing a potential ris 15 units 2010-03-08

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