BeneCath®

57 catalogue numbers from NC10M, listed by Hangzhou Jimushi Meditech Co., Ltd., China, under Catheter, Urethral. 11 manufacturers in China are registered for this product code.

Registry build 21.09.26
11manufacturers in China registered for this device type
57catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Zhejiang (6), Jiangsu (4), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code GBM
Manufacturer City Province Registered as Device types
Suzhou Jingle Polymer Medical Apparatus Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Integral Medical Products Co., Ltd. Shaoxing Zhejiang Contract manufacturer 7
Xianju Bever Medical Devices Co., Ltd. Taizhou Zhejiang Contract manufacturer 3
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Nanjing Anjian Medical Device Co., Ltd. Nanjing Jiangsu Contract manufacturer 22
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Hangzhou Jimushi Meditech Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Integral Sterilization Technology (Shaoxing) Co., Ltd. Shaoxing Zhejiang Contract manufacturer 5
Hangzhou Bever Medical Devices Co., Ltd. Hangzhou Zhejiang Specification developer 3
Xianju JF Medister Co., Ltd. Taizhou Zhejiang Contract manufacturer 2

Record

Regulatory record for BeneCath®
Listed by Hangzhou Jimushi Meditech Co., Ltd., China
FDA product code GBM
Device type Catheter, Urethral
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Contract manufacturer, Manufacturer
Record published 2021-01-01
Record revised 2020-12-25 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Box of 30, carton of 10

Catalogue Numbers

Catalogue numbers for BeneCath®
Catalogue number Size Status
NC10M In distribution
NCW12MC In distribution
NCH18M In distribution
NCH18MC In distribution
NCW18F In distribution
NCH12MC In distribution
NC14P In distribution
NC16P In distribution
NC10F In distribution
NC12P In distribution
NCH16MC In distribution
NCW08F In distribution
NC16MC In distribution
NCW14F In distribution
NCH14F In distribution
NCW14M In distribution
NCH16F In distribution
NC14F In distribution
NCW08M In distribution
NCH10F In distribution
NCW10P In distribution
NC16M In distribution
NC10P In distribution
NCH12M In distribution
NC08MC In distribution
NC12MC In distribution
NCW14MC In distribution
NCH08M In distribution
NC08P In distribution
NCH16M In distribution
NCW10F In distribution
NCW10M In distribution
NC14M In distribution
NC08F In distribution
NCH14M In distribution
NCW08MC In distribution
NC08M In distribution
NCH10MC In distribution
NCW12F In distribution
NC10MC In distribution
NCH12F In distribution
NCH14MC In distribution
NC12F In distribution
NC18M In distribution
NCW18M In distribution
NCW16M In distribution
NCW08P In distribution
NCH10M In distribution
NC12M In distribution
NC14MC In distribution
NCW12M In distribution
NCW18MC In distribution
NC18MC In distribution
NCW10MC In distribution
NCW16MC In distribution
NCW16F In distribution
NC16F In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SpeediCath Standard Coloplast A/S 47
TruCath HR Pharmaceuticals Inc. 46
VaPro Hollister Incorporated 31
Actreen® B. Braun Medical Inc. 28
McKesson Mckesson Medical-Surgical Inc. 25
BD Intermittent Hangzhou Bever Medical Devices Co., Ltd. 24
Gentlecath AIR Convatec, Purchasing Department 24
VaPro Pocket Hollister Incorporated 23
Apogee Hollister Incorporated 23
Dover Cardinal Health 23
Dover Cardinal Health 200, LLC 22
Teleflex Teleflex Medical LLC 22

Showing 12 of 76. All products under Catheter, Urethral

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K200134 2020-06-01

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