Hudson RCI

Universal Concha Column

Registry build 21.09.26
9manufacturers in China registered for this device type
1catalogue number
18recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Zhejiang (3), Guangdong (2). 6 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KOD
Manufacturer City Province Registered as Device types
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Guangdong Ecan Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 14
Clinisupplies (Nanjing) Co., Ltd. Nanjing Jiangsu Contract manufacturer 13
Integral Medical Products Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
Hangzhou Jimushi Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Integral Sterilization Technology (Shaoxing) Co., Ltd. Shaoxing Zhejiang Contract manufacturer 5

Record

Regulatory record for Hudson RCI
Listed by Teleflex Medical LLC, United States
FDA product code KOD
Device type Catheter, Urological
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K850335
Record published 2016-09-16
Record revised 2018-07-06 (version 4)

Specifications

Specifications
MRI safety MR Unsafe
Single use Yes
Latex Labelled latex-free
Packaging Box of 48

Catalogue Numbers

Catalogue numbers for Hudson RCI
Catalogue number Size Status
IPN044281 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rusch Teleflex Medical LLC 432
Dover Cardinal Health 200, LLC 163
Dover Cardinal Health 152
MTG HR Pharmaceuticals Inc. 59
Cook Cook Incorporated 43
Bardex® Lubricath® Foley Catheter C.R. Bard, Inc. 30
Magic3™ Intermittent Catheter C.R. Bard, Inc. 30
Ureteral Catheter Well Lead Medical Co., Ltd. 26
Bardex® Urethral Catheter Robinson Model C.R. Bard, Inc. 26
Personal Catheter™ Intermittent Catheter C.R. Bard, Inc. 24
DeRoyal Deroyal Industries, Inc. 23
Bard® Robinson Catheter C.R. Bard, Inc. 22

Showing 12 of 150. All products under Catheter, Urological

Recalls

5 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
2022-09-20 Class II Nonconforming Material/Component Product may not be sterile 7200 catheters
2019-07-01 Class II Equipment maintenance Potential for product not to be sterile. 3,700 devices 2021-11-04
2016-11-22 Class II Error in labeling Labeling Inconsistency: The products have been
labeled with the incorrect expiration date which exceeds the actual, validated 35-month shelf life.
102,843 units 2017-11-24
2014-09-04 Class II Labeling Change Control Misbranding: Although the product labeling identifies the catheters as “soft rubber,” the Natural Rubber Latex caution statement was not printed on the product label. 193,363 ea. + 1,140 units (total 194,503 units) 2017-02-22
2014-05-21 Class II Mixed-up of materials/components Product was packaged with a straight catheter rather than the correct coude (curved) catheter. 1000 eaches 2015-11-23
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. 14,378,890 units 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. see line 1. 2014-04-29
2011-06-30 Not classified Other Pin holes were detected in the packaging therefore sterility of the device can not be guaranteed. See line 1. 2014-04-29

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