Free Flow IJ

12.5F X 20CM IJ Free Flow Catheter SET W/Stylet W/2 Suture Wings

Registry build 21.09.26
2manufacturers in China registered for this device type
4catalogue numbers in this listing
8510(k) clearances naming this product code
5recalls on this code

Who Else Makes It

All of them in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MSD
Manufacturer City Province Registered as Device types
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6

Record

Regulatory record for Free Flow IJ
Listed by Medical Components Inc, United States
FDA product code MSD
Device type Catheter, Hemodialysis, Implanted
Device class Class 2
Regulation 21 CFR 876.5540
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-03-02
Record revised 2021-02-05 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for Free Flow IJ
Catalogue number Size Status
MFFS1520IJ In distribution
MFFS1512IJ In distribution
MFFS1515IJ In distribution
MFFS1220IJ-2 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 406
Split Cath® III Medical Components Inc 277
Palindrome Mozarc Medical US LLC 139
Titan HD Medical Components Inc 75
ProGuide™ Merit Medical Systems, Inc. 72
Hemo-Flow® Medical Components Inc 65
DuraMax® Merit Medical Systems, Inc. 55
CentrosFLO® Merit Medical Systems, Inc. 51
BioFlo DuraMax® Merit Medical Systems, Inc. 51
BioFlo Navilyst Medical, Inc. 45
DuraFlow AngioDynamics, Inc. 37
Mahurkar Mozarc Medical US LLC 37

Showing 12 of 123. All products under Catheter, Hemodialysis, Implanted

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121848 2012-09-21
K113487 2012-03-09
K111651 2011-12-08
K012562 2002-02-08
K994105 2001-10-03
K003207 2001-06-12
K981125 1999-02-26
K971925 1998-02-23

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
2020-07-27 Class II Under Investigation by firm Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer 132 eaches 2021-04-30
2015-02-05 Class II Process control Medcomp has initiated the recall of Duo-Flow 400XL Catheter, Hemo-Flow Catheter, SLX Catheter, Triple Lumen Infusion Catheter, CT rated PICC, Split Cath III, PC Split Cath III because the product shipped was out of specification. One BI (bi 3152 2015-08-06
2014-08-04 Class II Labeling False and Misleading The Split Cath III Trays were incorrectly labeled as 16F x 32CM Split Cath III instead of 28CM. 110 2014-12-10
2011-05-19 Not classified Mixed-up of materials/components Product was packaged with the incorrect valved peelable introducer. The catheter sized is 15.5F and the introducer packaged in the kit is a 15F. The kit should contain a 16F introducer. 90 2016-10-24
2009-09-02 Not classified Employee error mislabeled as right are actually left 100 trays 2010-04-16

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