SimPro™ Kit

Single Use Urinary Catheter with water sachet. Pediatric Nelaton 12" 08FR

Registry build 21.09.26
21manufacturers in China registered for this device type
12catalogue numbers in this listing
4510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (9), Zhejiang (7), Shanghai (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code EZD
Manufacturer City Province Registered as Device types
Conod Medical Co., Limited Changshu Jiangsu Contract manufacturer 48
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Conod Medical Shuyang Co., Ltd. Shuyang Jiangsu Contract manufacturer 22
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Haiyan Kangyuan Medical Instrument Co., Ltd. Jiaxing Zhejiang Contract manufacturer 17
Jiangsu Suyun Medical Materials Co., Ltd. Lianyungang Jiangsu Contract manufacturer 11
Integral Medical Products Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
Shaoxing Fuqing Health Products Co., Ltd. Shaoxing Zhejiang Contract manufacturer 3
Xianju Bever Medical Devices Co., Ltd. Taizhou Zhejiang Contract manufacturer 3
Sterigenics Shanghai ETO Ltd. Shanghai Shanghai Contract manufacturer 65
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Changshu Rozer Sterilization Technology Co., Ltd. Changshu Jiangsu Contract manufacturer 43

Showing 12 of 21. All 21 manufacturers in China registered for Catheter, Straight

Record

Regulatory record for SimPro™ Kit
Listed by Wellspect Healthcare, Sweden
FDA product code EZD
Device type Catheter, Straight
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Contract manufacturer, Contract steriliser, Specification developer, Manufacturer
Record published 2019-02-26
Record revised 2023-03-30 (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
Storage Special storage condition: Store in a dry place at room temperature.
Packaging Pack of 4, pack of 20
Sizes Catheter gauge 8 to 16 Fr; length 8 to 16 in
Distribution end date 2022-04-14

Catalogue Numbers

Catalogue numbers for SimPro™ Kit
Catalogue number Size Status
5201600 Catheter Gauge 16 Fr Withdrawn
5231600 Length 8 in Withdrawn
5220800 Catheter Gauge 8 Fr Withdrawn
5221000 Catheter Gauge 10 Fr Withdrawn
5201000 Catheter Gauge 10 Fr Withdrawn
5201400 Length 16 in Withdrawn
5231200 Length 8 in Withdrawn
5231000 Length 8 in Withdrawn
5201200 Length 16 in Withdrawn
5200800 Catheter Gauge 8 Fr Withdrawn
5231400 Length 8 in Withdrawn
5230800 Length 8 in Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Disposable intermittent catheter (TPU Catheter) Chengdu Daxan Innovative Medical Tech. Co., Ltd. 140
LoFric® Hydro-Kit™ Wellspect Healthcare 57
LoFric® Wellspect Healthcare 56
SimPro™ Now Wellspect Healthcare 55
Self-Cath Coloplast A/S 50
Wellead PVC Hydrophilic Urethral Catheter Well Lead Medical Co., Ltd. 50
LoFric® Primo™ Wellspect Healthcare 48
Medline Medline Industries, Inc. 47
Halyard Owens & Minor Distribution, Inc. 39
Cure Catheter Convatec, Purchasing Department 39
AMSure® PVC Intermittent Catheter Amsino Medical Inc. 39
LoFric® Origo™ Wellspect Healthcare 34

Showing 12 of 72. All products under Catheter, Straight

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261658 2026-07-17
K260999 2026-04-24
K250659 2025-09-26
K123751 2013-02-28

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 Closed
2020-06-17 Class II Equipment maintenance Wellspect Healthcare is voluntarily recalling certain LoFric Origo” urethral catheters due to a potential defect which may be present in the catheter s distal tip. 2021-04-09
2020-06-17 Class II Equipment maintenance Wellspect Healthcare is voluntarily recalling certain LoFric Origo” urethral catheters due to a potential defect which may be present in the catheters distal tip. 2021-04-09
2020-06-17 Class II Equipment maintenance Wellspect Healthcare is voluntarily recalling certain LoFric Origo” urethral catheters due to a potential defect which may be present in the catheters distal tip. 2021-04-09

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