VaPro Plus Pocket

No Touch Urethral Intermittent Catheter with Integrated Collection Bag, Hydrophilic, Straight Tip, Protective Tip and Sleeve

Registry build 21.09.26
11manufacturers in China registered for this device type
18catalogue numbers in this listing
11510(k) clearances naming this product code

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 VaPro Plus Pocket
Listed by Hollister Incorporated, United States
FDA product code GBM
Device type Catheter, Urethral
Device class Class 2
Regulation 21 CFR 876.5130
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer
510(k) K233524
Record published 2024-06-26
Record revised 2024-06-04 (version 7)

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, manufacturing date
Storage Storage environment temperature 15 to 30 °C
Packaging Case of 4, box of 30
Sizes Catheter gauge 8 to 16 Fr; catheter length 20 to 40 cm; length 8 to 16 in
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for VaPro Plus Pocket
Catalogue number Size Per pack Status
71144 Catheter Length 40 cm 30 In distribution
71164-30 Length 16 in 30 In distribution
71102-30 Catheter Gauge 10 Fr 30 In distribution
71082 Catheter Length 20 cm 30 In distribution
71142-30 Catheter Gauge 14 Fr 30 In distribution
71144-30 Catheter Gauge 14 Fr In distribution
71124-30 Catheter Gauge 12 Fr 30 In distribution
71082-30 Length 8 in 30 In distribution
71122-30 Length 8 in In distribution
71164 Catheter Length 40 cm 30 In distribution
71124 Catheter Gauge 12 Fr 30 In distribution
71084 Catheter Length 40 cm 30 In distribution
71104 Catheter Length 40 cm 30 In distribution
71122 Catheter Gauge 12 Fr 30 In distribution
71104-30 Length 16 in 30 In distribution
71102 Catheter Gauge 10 Fr 30 In distribution
71084-30 Length 16 in 30 In distribution
71142 Catheter Gauge 14 Fr 30 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
BeneCath® Hangzhou Jimushi Meditech Co., Ltd. 57
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

Showing 12 of 76. All products under Catheter, Urethral

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211436 2022-01-27
K193148 2019-12-13
K191633 2019-07-19
K183253 2018-12-18
K180824 2018-06-22
K163179 2017-01-26
K152268 2015-09-09
K143594 2015-01-09
K141642 2014-08-22
K110862 2011-04-26
K090960 2009-08-20

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